Tag | Content |
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EnhancerAtlas ID | HS136-07797 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr17:997690-1002310 |
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 | chr17:997865-1000627 | Gastric | SE_40640 | chr17:1001472-1002187 | Left_Ventricle | SE_40640 | chr17:997883-1000658 | Left_Ventricle | SE_42080 | chr17:997890-999987 | LNCaP | SE_42145 | chr17:1000796-1001386 | Lung | 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: 7 | Chromosome | Start | End |
chr17 | 999488 | 999757 | chr17 | 1001002 | 1001184 | chr17 | 1001580 | 1002074 | chr17 | 998333 | 998651 | chr17 | 998689 | 1000165 | chr17 | 998903 | 999111 | chr17 | 998449 | 998620 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I001094 | chr17 | 997981 | 1002712 |
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Enhancer Sequence | ACCTCCGCCT CCCAGGTTCA AGCGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGAATTA 60 CAGGTGTCCA CCACCCCGCC CAGCTAGTTT TTGTAGTTTT TGTAGATATG GGGTTTCACC 120 ATATTGGTCA GGCTGGTCTC AAACTCCTGA CTTCAAGTGA TCCACGTGCC TCGGCCTCTT 180 GAAGTGCTGG GATGACAGGT GTTGAGCCAC CATGCCTGGC TGAGACCTTT ATAATCCAGT 240 TGGGCAAAAT GGGCCAACAC AGATGAAATG ACTATGGACG ATGCGACTGA CTGTAAGCAC 300 CAACCACATG GTTCCAAGGT TGTGCTGGAG TAGCCTGGAG GGCTGCATGG AGGAGGCACA 360 CATACCAGGT CCTTGGAGAG CTGAGCAGGT GGAGGAGTGG GGGCGTAGAG AGGCATGCCA 420 GACAGGGAAA CAGAAGGCAC CGGGAGGCAG GAGCAAGGGA AGAGTGTCCC CCCAAGCCCA 480 GGTGGGTGAG CTGAAAGCTT TGGGGACTCC CCACCCTCCA TGAGGGACAT GGAACTAGCT 540 TCAGGATTGA CATCGTCGTA AGAGTTTATC CTTTTCACCT CAACGCAGGA CCCCACGGAG 600 GAGCCCGCAG AGTCGCCACA GAATCCCCAT ACCCAAGAAT TCTTGTCCCC GCCTTGGCGC 660 AGTCCCCACT GAGGGGGAAA TAAGGGAAGC AGGAAGGTCA GCAGTCCCAG GAAGGCCAAG 720 GAGACGGGAT TTCTCAGAAG CCGCGACGCG CTCATCTGCC ACCCACACGA AGACAAAACA 780 CAATGGTTAT GCTTCCTCCT CAACTTCCCA CCCCGTCTGC AAAAGGGGAA GAAATGGACG 840 CTCACCCACA GCCAGTCACA AGGACGGGGC CTGCGCTTGG GGCATCAGAT GGTTCTCATG 900 ACACGATGGG GACCTTGGCT GTTACTCCTG ATTTCACTCG CGGGGAGGGG ACAGGGCTGG 960 GTGTGTGCCC TTGGCTGGCC AGGACCCTCG AGGCCGTTAT TTGTCTCTGG TGAAGTCCTG 1020 CGTATGGGCT CAGGGGCAGG AGGGTGGACT GAAAGGCAAG GTGACCCACA CTGAGCTTCG 1080 GCACGGCACA GCCATTCTGC CAAAGCGCTA GCACACCACT CAGGCACCCC CTCCTCCCCA 1140 GTCCTGCTGC AGGGACAAGG GCAGGCCCCG GCTCTCCATT TCACCACTCG AGTTCTCGGA 1200 GAGGACCCGT GAGTGACTTC AACCCTGGCT CCCATACCAG CTGCTTCTCA GGAAGACGGG 1260 CCTGGGCCGG TTCTCACTTG CCAGTGGGAC TTCACATAGC CGTTTGTCAG CTCTGTCCCC 1320 CAGCGACCGG CCTTTCGAAA TAAGGGAAAG AAATGTACCC ACTTCCTCCA CCTCCTGCCC 1380 CAGAAGGCCT GGCATGCTTG CTGCCATGCC ACCCGAGTCA CTCGTCACTG GAGCCCAGGG 1440 AGGAAGGCCT CATTCACCTG TTTTATAGAT AAAGAGCCTG CGATGCAGCG TGGCCAGGAG 1500 TCCACCCCAG GAGGGCCAGT CGTGGCCAGC GGTGGGAGGG GCTCTGGGGA GTGGCCTCAC 1560 CCTGTGGCCC CAGCGTAGCA AGACACAGTT CCCAAGCTCA GTTCCCAGTG TCAAGGAGAT 1620 CCAGAATTTC AATGCAGTTG GCTTCATCTT TTTTCCTTCA CCCCCTACTT CGGCCCAGGC 1680 TCCCAGGCTT TTCCTGTAAT CAGAGCCCAC CAGGAAGCAG GAGGGCCCCA GAAGATGACC 1740 CCCACAAGCA CCCCAGAGGC CAGGACGGAG GCTTCTGTGT GGAGGCTCGT CTGCCCCGTG 1800 TGTGCACATG GTTTTAGGTA CACACACCCA GCCCTTTGCA TATCAGGAAG TGTTCAGATG 1860 AAAGCAAACA GGCTGGGGCA GAGCGGTGGG AATGGGGTCA GGAGTGGGAA AGCGAGCATG 1920 GAGGGAACGA ATTTCTTCTC CTTCAAGCTG GCACCTTTGC GAGGCCACCC CGAAGAGCAG 1980 AAGGTTTAGC TTCCTCCTAG CTGAGGGGTG GGGAGGGTGC AGGGGTTCCC AGCTCAGGGA 2040 GGAGAGGAGG AAGGGTGTGA TTCTTTCACT CTGAGGTTTT CTTCTGAGGC TGTGGCTGTG 2100 GAGGGTCCTA CTCCTCTTCC TGAGCCCTCC TACCACAGAC CTGGCCTCCC AGCGAGTTCT 2160 TCCTTTGCTC CCTCTGGTCT CTGCTCAAGA AAGAGCCAAG CAGGGGCCCA GGAGGAGAGA 2220 GCTGGGGGAA GGTGGGGAAC CCGCCCCGGG AGGAGAGAGC TGGGGAAGGG GGGGAACCTG 2280 CCCCGGGAGG AGAGAGCTGG GGAAGGGGGG AACCTGCCCC GGGTGGAGAG AGCTGGGGGA 2340 AGTGGGGGAA CCTGCCCCGG GAGGAGAGAG CTGGGGAAGG GGGGAAACCT GCCCCAGGAG 2400 AGAGCTGGGG AATGGGGGAA CCTGCCCCAG GAGGAGACAG CTGGGGAAGG GGGGAAACCT 2460 GCCCCGGGAG AGAGCTGGGG AAGGGGGGAA CCTGCCCGGG GAGGAGAGAG CCGGGGAAGG 2520 GGGGAACCTG CCCCGGGAGG AGACAGCTGG GGAAGGGGGG AACCTGCGCC AGGCATATCA 2580 GGAAGGGGGC CCCTGCCCCA CAGATTCTGC CTTTGGGGCA TGAGCTGTTA GAAAGGCAGA 2640 GCAGGGAGGG GCTCTTGGTC TTGGCCCAGA GGAAGAGGCT CGTGGGTGGC AGGTGGGATC 2700 TAAGGGCTCC GTGTCTGATG GGGACAGGCG CCACTCCCTC CTTCAGGGAA CGGGTGTGTT 2760 GTGGCAGAAA CCACGAAGCC CTAACCTGTC TCCTCTCCCA GCAATAGAGA AATTAACAGT 2820 GTCAACGAAC ACTCAGGCTG TGTTCTAAGA GCTTTATGTG CCGGACACAG TGGCTCACAT 2880 CTGTAATCCC AGCACTTTGG GAGGCCGAGG CGGGCGGATC ACTTGAGGTC AGGAGTTCAA 2940 GACCAGCCTG GCCAACATGG TGAAATCTCA TCTCTACTAA AAATACAAAA ATTAGCTGGG 3000 CGTGGTGGTG GGTGCCTGTA ATCTCAGCTA CTTGGGAAGC TGACACAGGA GAATGGCTTG 3060 AACCCAGGAG GCGGAGGTTA TAATGAGCCG AGATTGTGCC ACTGCACTCC AGCCTGGGCA 3120 ACAGAGCAAG ACTCCGTCTC AAAAAAAAAA AAAAAAAAAG AACTCTGTGT ATAAATTCCT 3180 TTAATCCTCA CAACGACCCC ATGAAAAGCA TACTATTTGT ATACCCAGTT TGCAGATGGA 3240 AAAACTGAGG CACGATAGCT CATTCACCTG CTGAAAGCCT GGAGCCAGTA CGGCCAGGCA 3300 GTCTAGATCC TCTGTCTGAA CTCCTTTCAA ATACACACCC TGTTAGTAAT GACAACTATG 3360 TTCCTTTTTG GACAGCAATT CACGGTTTGG AAGACGTGTT TCACGAATGT CTGACGGGTT 3420 GTCTCTTTGC CTGTCCTCCT TTCTTCCACT AACAGTTGAG TGTCTTAAGT AACTCAACGC 3480 TGTATGAGGT CCCGAAAGCA TCTCCCGATC TTCTCAACCC CATGGAAAGA GAGAGAAAGA 3540 ATGGCATCCC TCTCATCTTC AGATCCAGAA ATGGAGGCTC AAGGAATTTA TGTAGGGCTT 3600 GCCCAAAGCC AGCAGTTTTC TTTTCTTTTT TTTTTTTTTT GTGATGGAGT CTCACTGTGT 3660 CGCCCAGGCT GGAGTGCAGT GGCGCAATCT CTGCTCACTG CAAGCTCCGC CTCCCAGGTT 3720 GACGCCATTC TCCTGCCTCA GCCTCCCGAG TGGCTGGGAC TACAGGTGCT CGCCACCACG 3780 CCCGGCTAAT TTTTTTTGTA CTTTTTTAGT AGAGACGGGG TTTCACCGTG TTGGCCAAGG 3840 ATGGTCTGGA TCTCCTGACC TTGTGATCCG CCCACCTCAG CCTCCCAAAG TGCTGGGATT 3900 ACAGGCTTGA GACACGGCGC CCGGCCAAAG CCAGCAGTTT TCAAACCCAC AACAGGTGTA 3960 AGACACCATG GGCCCGGCAA TTACATATAT ATACAGGCAC ACAGACAGAC AACAAACCGA 4020 AAGTTCCCTC ACTTATCTTT CCCGTGTATG ATGCATGCTG ACATTTTTTC ATTGGTTTAA 4080 AAATGCTGGT TCAACCCACT GTACTGGTTT CACAACCCAC TGTACTGATT TCACAACCCA 4140 AAGCACTGAT GGGCTGAGAG GCACAGTTTG AGAAACAGTG CAATACGCCT GCTCTTAATG 4200 GCAGGGCCAA GTCTTGCCCT AGCTCTGGCC CCAGACCAGG ACCCTCAGCT ACCTGCCACA 4260 CTGCCCCTCA CTTGGAAAAC AGCTCCGTAC ACACAGATAA ACTCCTGGAG AGATGGGACG 4320 TACTCAGCCT GGCGTGTGGC AAAACAGCTG CACATTCAGA GTTTCACTCT TGTTGCCCCG 4380 GCTGGAGTGC AATGGTGCAA ACTCGGCTCA CTGCAACCTC CACCTCCCGG GTTCAAGCGA 4440 TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGG GCCCGCCACC ACGCCCAGCT 4500 AATTTTTTGT ATTTTTAGTA GAGATGGGGC TTCACCATGT TGGCCAGGCT GGTCTCGAAC 4560 TCCTGACCTC AGGTGATCCA CCCACCTCGG CCTCCCAAAG TGCTGGGATT ACAGGTGTCA 4620
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