Tag | Content |
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EnhancerAtlas ID | HS017-13025 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr17:996830-1002760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:999726-999744 | GGGAGGAGAGGAGGAAGG | + | 6.05 | Nr2f6(var.2) | MA0728.1 | chr17:1000614-1000629 | GAGGTCAGGAGTTCA | + | 6.22 | SPIC | MA0687.1 | chr17:998509-998523 | CAAAAGGGGAAGAA | + | 6.21 | Stat6 | MA0520.1 | chr17:998932-998947 | GCTTCTCAGGAAGAC | - | 6.12 | ZNF263 | MA0528.1 | chr17:999050-999071 | ACTTCCTCCACCTCCTGCCCC | - | 6.23 | Zfx | MA0146.2 | chr17:1000590-1000604 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_09651 | chr17:997459-1003314 | CD14 | SE_23220 | chr17:998840-1000622 | Colon_Crypt_1 | SE_23794 | chr17:998552-1000541 | Colon_Crypt_2 | SE_24832 | chr17:998496-1000617 | Colon_Crypt_3 | SE_26634 | chr17:1001416-1002150 | Esophagus | SE_26634 | chr17:998039-1001385 | Esophagus | SE_28034 | chr17:1000814-1002370 | Fetal_Intestine | SE_28034 | chr17:998534-1000478 | Fetal_Intestine | SE_29195 | chr17:1000681-1002526 | Fetal_Intestine_Large | SE_29195 | chr17:998712-1000655 | Fetal_Intestine_Large | SE_31579 | chr17:996682-997612 | Gastric | SE_31579 | chr17:997865-1000627 | Gastric | SE_40640 | chr17:1001472-1002187 | Left_Ventricle | SE_40640 | chr17:997883-1000658 | Left_Ventricle | SE_42080 | chr17:997890-999987 | LNCaP | SE_42145 | chr17:1001451-1002180 | Lung | SE_42145 | chr17:997788-1000650 | Lung | SE_49097 | chr17:997877-1000027 | Right_Atrium | SE_49495 | chr17:998380-999678 | Right_Ventricle | SE_50313 | chr17:997764-1000663 | Sigmoid_Colon | SE_52631 | chr17:998424-1000653 | Small_Intestine | SE_54272 | chr17:1000739-1001441 | Spleen | SE_54272 | chr17:1001470-1002169 | Spleen | SE_54272 | chr17:997807-1000601 | Spleen | SE_65254 | chr17:997895-1000753 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 9 | Chromosome | Start | End |
chr17 | 999488 | 999757 | chr17 | 1001002 | 1001184 | chr17 | 1001580 | 1002074 | chr17 | 997015 | 997152 | chr17 | 997454 | 997598 | chr17 | 998333 | 998651 | chr17 | 998689 | 1000165 | chr17 | 998903 | 999111 | chr17 | 998449 | 998620 |
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| Number: 2 | ID | Chromosome | Start | End |
GH17I001093 | chr17 | 996472 | 997612 | GH17I001094 | chr17 | 997981 | 1002712 |
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Enhancer Sequence | GCTTTCCGAC AAGAGAAGCA TTCTAGCAGA GAATGGGTGA CTCCACTGCT GAAAATGCTG 60 CACTGAAGGG AACACCAAAG CCAGCGCCAG CTCCCTCTGA ACGACGACCA CCAGCTCCAG 120 CCAACCACGG CAAACTCCCA GCCCAGCCTC ACTCCAGCCT CACATCACCT CATTCTGATG 180 AAGTCTCATC TACTCAGATA TATCGCCTCA CTCTGATGGA GACAGAACCC ATGTTCACTG 240 GAAGAAGTCG TCTCATCTAC TCAGACACCC AGATGGTGCT CTGCCTTCTG GCTCCTTCAT 300 CCTCCGAGCT CTAAAAAGCC CAGATCCAAC AATCCATGCA GGACAAAGCA GGACCCTCCT 360 TCTGACCCTC GCCGCGCTAG AAACAACGGC CCCTCAGTGT CCAGTCAGGA CTCTCCTTCT 420 GACCCTCGCT GTGCTAGAAT CAATGGCCCC TCGGTGTCCG GTCAGGCCCC TCCTTCTGAC 480 CCTCACCGTC CTAGAACCAA CGGCCCCTCT GCGTCCGGTC AGGCCTCTCC TTCTGACCCT 540 CGCCGTCCTA GAACCAACGG CCCCTCGGTG TCTGGTCCTT GCTAGGCAAG CGCATGGGGT 600 TCCACCTGGT GCAGGCCAGG CAGGGTGGGC TTGAGTCGCA GCTCTGCTGT GCGCACATCA 660 CTCAGCATCC CTGGGCTTCG TGTCACCAGC AGCCTCATGT GTGAAACTGG GATAATACAG 720 CCATGCGCTA CCTACTGGCA TTCCCGTCAG TGCGTACACG ATCATGGTCC CAGACTGCAA 780 TTTTTTTTTT TTTTTTTTGA GACAGAGTCT CACTCTGTCA CCCAGGCTGG AGTGCAATAG 840 TGCAATCTCG GCTCACTGCA ACCTCCGCCT CCCAGGTTCA AGCGATTCTC CTGCCTCAGC 900 CTCCTGAGTA GCTGGAATTA CAGGTGTCCA CCACCCCGCC CAGCTAGTTT TTGTAGTTTT 960 TGTAGATATG GGGTTTCACC ATATTGGTCA GGCTGGTCTC AAACTCCTGA CTTCAAGTGA 1020 TCCACGTGCC TCGGCCTCTT GAAGTGCTGG GATGACAGGT GTTGAGCCAC CATGCCTGGC 1080 TGAGACCTTT ATAATCCAGT TGGGCAAAAT GGGCCAACAC AGATGAAATG ACTATGGACG 1140 ATGCGACTGA CTGTAAGCAC CAACCACATG GTTCCAAGGT TGTGCTGGAG TAGCCTGGAG 1200 GGCTGCATGG AGGAGGCACA CATACCAGGT CCTTGGAGAG CTGAGCAGGT GGAGGAGTGG 1260 GGGCGTAGAG AGGCATGCCA GACAGGGAAA CAGAAGGCAC CGGGAGGCAG GAGCAAGGGA 1320 AGAGTGTCCC CCCAAGCCCA GGTGGGTGAG CTGAAAGCTT TGGGGACTCC CCACCCTCCA 1380 TGAGGGACAT GGAACTAGCT TCAGGATTGA CATCGTCGTA AGAGTTTATC CTTTTCACCT 1440 CAACGCAGGA CCCCACGGAG GAGCCCGCAG AGTCGCCACA GAATCCCCAT ACCCAAGAAT 1500 TCTTGTCCCC GCCTTGGCGC AGTCCCCACT GAGGGGGAAA TAAGGGAAGC AGGAAGGTCA 1560 GCAGTCCCAG GAAGGCCAAG GAGACGGGAT TTCTCAGAAG CCGCGACGCG CTCATCTGCC 1620 ACCCACACGA AGACAAAACA CAATGGTTAT GCTTCCTCCT CAACTTCCCA CCCCGTCTGC 1680 AAAAGGGGAA GAAATGGACG CTCACCCACA GCCAGTCACA AGGACGGGGC CTGCGCTTGG 1740 GGCATCAGAT GGTTCTCATG ACACGATGGG GACCTTGGCT GTTACTCCTG ATTTCACTCG 1800 CGGGGAGGGG ACAGGGCTGG GTGTGTGCCC TTGGCTGGCC AGGACCCTCG AGGCCGTTAT 1860 TTGTCTCTGG TGAAGTCCTG CGTATGGGCT CAGGGGCAGG AGGGTGGACT GAAAGGCAAG 1920 GTGACCCACA CTGAGCTTCG GCACGGCACA GCCATTCTGC CAAAGCGCTA GCACACCACT 1980 CAGGCACCCC CTCCTCCCCA GTCCTGCTGC AGGGACAAGG GCAGGCCCCG GCTCTCCATT 2040 TCACCACTCG AGTTCTCGGA GAGGACCCGT GAGTGACTTC AACCCTGGCT CCCATACCAG 2100 CTGCTTCTCA GGAAGACGGG CCTGGGCCGG TTCTCACTTG CCAGTGGGAC TTCACATAGC 2160 CGTTTGTCAG CTCTGTCCCC CAGCGACCGG CCTTTCGAAA TAAGGGAAAG AAATGTACCC 2220 ACTTCCTCCA CCTCCTGCCC CAGAAGGCCT GGCATGCTTG CTGCCATGCC ACCCGAGTCA 2280 CTCGTCACTG GAGCCCAGGG AGGAAGGCCT CATTCACCTG TTTTATAGAT AAAGAGCCTG 2340 CGATGCAGCG TGGCCAGGAG TCCACCCCAG GAGGGCCAGT CGTGGCCAGC GGTGGGAGGG 2400 GCTCTGGGGA GTGGCCTCAC CCTGTGGCCC CAGCGTAGCA AGACACAGTT CCCAAGCTCA 2460 GTTCCCAGTG TCAAGGAGAT CCAGAATTTC AATGCAGTTG GCTTCATCTT TTTTCCTTCA 2520 CCCCCTACTT CGGCCCAGGC TCCCAGGCTT TTCCTGTAAT CAGAGCCCAC CAGGAAGCAG 2580 GAGGGCCCCA GAAGATGACC CCCACAAGCA CCCCAGAGGC CAGGACGGAG GCTTCTGTGT 2640 GGAGGCTCGT CTGCCCCGTG TGTGCACATG GTTTTAGGTA CACACACCCA GCCCTTTGCA 2700 TATCAGGAAG TGTTCAGATG AAAGCAAACA GGCTGGGGCA GAGCGGTGGG AATGGGGTCA 2760 GGAGTGGGAA AGCGAGCATG GAGGGAACGA ATTTCTTCTC CTTCAAGCTG GCACCTTTGC 2820 GAGGCCACCC CGAAGAGCAG AAGGTTTAGC TTCCTCCTAG CTGAGGGGTG GGGAGGGTGC 2880 AGGGGTTCCC AGCTCAGGGA GGAGAGGAGG AAGGGTGTGA TTCTTTCACT CTGAGGTTTT 2940 CTTCTGAGGC TGTGGCTGTG GAGGGTCCTA CTCCTCTTCC TGAGCCCTCC TACCACAGAC 3000 CTGGCCTCCC AGCGAGTTCT TCCTTTGCTC CCTCTGGTCT CTGCTCAAGA AAGAGCCAAG 3060 CAGGGGCCCA GGAGGAGAGA GCTGGGGGAA GGTGGGGAAC CCGCCCCGGG AGGAGAGAGC 3120 TGGGGAAGGG GGGGAACCTG CCCCGGGAGG AGAGAGCTGG GGAAGGGGGG AACCTGCCCC 3180 GGGTGGAGAG AGCTGGGGGA AGTGGGGGAA CCTGCCCCGG GAGGAGAGAG CTGGGGAAGG 3240 GGGGAAACCT GCCCCAGGAG AGAGCTGGGG AATGGGGGAA CCTGCCCCAG GAGGAGACAG 3300 CTGGGGAAGG GGGGAAACCT GCCCCGGGAG AGAGCTGGGG AAGGGGGGAA CCTGCCCGGG 3360 GAGGAGAGAG CCGGGGAAGG GGGGAACCTG CCCCGGGAGG AGACAGCTGG GGAAGGGGGG 3420 AACCTGCGCC AGGCATATCA GGAAGGGGGC CCCTGCCCCA CAGATTCTGC CTTTGGGGCA 3480 TGAGCTGTTA GAAAGGCAGA GCAGGGAGGG GCTCTTGGTC TTGGCCCAGA GGAAGAGGCT 3540 CGTGGGTGGC AGGTGGGATC TAAGGGCTCC GTGTCTGATG GGGACAGGCG CCACTCCCTC 3600 CTTCAGGGAA CGGGTGTGTT GTGGCAGAAA CCACGAAGCC CTAACCTGTC TCCTCTCCCA 3660 GCAATAGAGA AATTAACAGT GTCAACGAAC ACTCAGGCTG TGTTCTAAGA GCTTTATGTG 3720 CCGGACACAG TGGCTCACAT CTGTAATCCC AGCACTTTGG GAGGCCGAGG CGGGCGGATC 3780 ACTTGAGGTC AGGAGTTCAA GACCAGCCTG GCCAACATGG TGAAATCTCA TCTCTACTAA 3840 AAATACAAAA ATTAGCTGGG CGTGGTGGTG GGTGCCTGTA ATCTCAGCTA CTTGGGAAGC 3900 TGACACAGGA GAATGGCTTG AACCCAGGAG GCGGAGGTTA TAATGAGCCG AGATTGTGCC 3960 ACTGCACTCC AGCCTGGGCA ACAGAGCAAG ACTCCGTCTC AAAAAAAAAA AAAAAAAAAG 4020 AACTCTGTGT ATAAATTCCT TTAATCCTCA CAACGACCCC ATGAAAAGCA TACTATTTGT 4080 ATACCCAGTT TGCAGATGGA AAAACTGAGG CACGATAGCT CATTCACCTG CTGAAAGCCT 4140 GGAGCCAGTA CGGCCAGGCA GTCTAGATCC TCTGTCTGAA CTCCTTTCAA ATACACACCC 4200 TGTTAGTAAT GACAACTATG TTCCTTTTTG GACAGCAATT CACGGTTTGG AAGACGTGTT 4260 TCACGAATGT CTGACGGGTT GTCTCTTTGC CTGTCCTCCT TTCTTCCACT AACAGTTGAG 4320 TGTCTTAAGT AACTCAACGC TGTATGAGGT CCCGAAAGCA TCTCCCGATC TTCTCAACCC 4380 CATGGAAAGA GAGAGAAAGA ATGGCATCCC TCTCATCTTC AGATCCAGAA ATGGAGGCTC 4440 AAGGAATTTA TGTAGGGCTT GCCCAAAGCC AGCAGTTTTC TTTTCTTTTT TTTTTTTTTT 4500 GTGATGGAGT CTCACTGTGT CGCCCAGGCT GGAGTGCAGT GGCGCAATCT CTGCTCACTG 4560 CAAGCTCCGC CTCCCAGGTT GACGCCATTC TCCTGCCTCA GCCTCCCGAG TGGCTGGGAC 4620 TACAGGTGCT CGCCACCACG CCCGGCTAAT TTTTTTTGTA CTTTTTTAGT AGAGACGGGG 4680 TTTCACCGTG TTGGCCAAGG ATGGTCTGGA TCTCCTGACC TTGTGATCCG CCCACCTCAG 4740 CCTCCCAAAG TGCTGGGATT ACAGGCTTGA GACACGGCGC CCGGCCAAAG CCAGCAGTTT 4800 TCAAACCCAC AACAGGTGTA AGACACCATG GGCCCGGCAA TTACATATAT ATACAGGCAC 4860 ACAGACAGAC AACAAACCGA AAGTTCCCTC ACTTATCTTT CCCGTGTATG ATGCATGCTG 4920 ACATTTTTTC ATTGGTTTAA AAATGCTGGT TCAACCCACT GTACTGGTTT CACAACCCAC 4980 TGTACTGATT TCACAACCCA AAGCACTGAT GGGCTGAGAG GCACAGTTTG AGAAACAGTG 5040 CAATACGCCT GCTCTTAATG GCAGGGCCAA GTCTTGCCCT AGCTCTGGCC CCAGACCAGG 5100 ACCCTCAGCT ACCTGCCACA CTGCCCCTCA CTTGGAAAAC AGCTCCGTAC ACACAGATAA 5160 ACTCCTGGAG AGATGGGACG TACTCAGCCT GGCGTGTGGC AAAACAGCTG CACATTCAGA 5220 GTTTCACTCT TGTTGCCCCG GCTGGAGTGC AATGGTGCAA ACTCGGCTCA CTGCAACCTC 5280 CACCTCCCGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGG 5340 GCCCGCCACC ACGCCCAGCT AATTTTTTGT ATTTTTAGTA GAGATGGGGC TTCACCATGT 5400 TGGCCAGGCT GGTCTCGAAC TCCTGACCTC AGGTGATCCA CCCACCTCGG CCTCCCAAAG 5460 TGCTGGGATT ACAGGTGTCA GCCACTGCAC CCAGCCTTTT TTTTTGAGGA ATTTCACTTC 5520 CGTCGTCCAG TCTGGAGTAC AGTGGCGCAC TCTCAGCTCA CTACGACCTT CGCCCCCAGA 5580 TTCAAGCAAT TCTCATGCCT CAGCCTCCTG AGTAACTGGG ATTACAGGTA TGCACCACCA 5640 CGCCTGGCTT TTTTTTGCAT TTCTAGCAGA GACAAGGTTT CACCACATTG GCCAGGCTGG 5700 TCTCGAACTC CTGTCCTCAA GTGATCTGCC CACCTGGGGC TCCCAAAGTG CTGGGATTAC 5760 AGGCACTGAG CCACGGCGCC CGGCCTGCAC CTGCACATTT ACACAGTCAT TCCTGGGTAA 5820 CATAAATGTC AAGTCCCCTG GGACACTGAC AGCATCTCAG GGTTGACGTG TGACAACACC 5880 TCACGTCATG GCAAGTACTT AAATGTGCAT CTTAGAATTC TTGTTAAGAA 5930
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