Tag | Content |
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EnhancerAtlas ID | HS023-10042 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr17:997780-1002420 |
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 | TTGTAGTTTT TGTAGATATG GGGTTTCACC ATATTGGTCA GGCTGGTCTC AAACTCCTGA 60 CTTCAAGTGA TCCACGTGCC TCGGCCTCTT GAAGTGCTGG GATGACAGGT GTTGAGCCAC 120 CATGCCTGGC TGAGACCTTT ATAATCCAGT TGGGCAAAAT GGGCCAACAC AGATGAAATG 180 ACTATGGACG ATGCGACTGA CTGTAAGCAC CAACCACATG GTTCCAAGGT TGTGCTGGAG 240 TAGCCTGGAG GGCTGCATGG AGGAGGCACA CATACCAGGT CCTTGGAGAG CTGAGCAGGT 300 GGAGGAGTGG GGGCGTAGAG AGGCATGCCA GACAGGGAAA CAGAAGGCAC CGGGAGGCAG 360 GAGCAAGGGA AGAGTGTCCC CCCAAGCCCA GGTGGGTGAG CTGAAAGCTT TGGGGACTCC 420 CCACCCTCCA TGAGGGACAT GGAACTAGCT TCAGGATTGA CATCGTCGTA AGAGTTTATC 480 CTTTTCACCT CAACGCAGGA CCCCACGGAG GAGCCCGCAG AGTCGCCACA GAATCCCCAT 540 ACCCAAGAAT TCTTGTCCCC GCCTTGGCGC AGTCCCCACT GAGGGGGAAA TAAGGGAAGC 600 AGGAAGGTCA GCAGTCCCAG GAAGGCCAAG GAGACGGGAT TTCTCAGAAG CCGCGACGCG 660 CTCATCTGCC ACCCACACGA AGACAAAACA CAATGGTTAT GCTTCCTCCT CAACTTCCCA 720 CCCCGTCTGC AAAAGGGGAA GAAATGGACG CTCACCCACA GCCAGTCACA AGGACGGGGC 780 CTGCGCTTGG GGCATCAGAT GGTTCTCATG ACACGATGGG GACCTTGGCT GTTACTCCTG 840 ATTTCACTCG CGGGGAGGGG ACAGGGCTGG GTGTGTGCCC TTGGCTGGCC AGGACCCTCG 900 AGGCCGTTAT TTGTCTCTGG TGAAGTCCTG CGTATGGGCT CAGGGGCAGG AGGGTGGACT 960 GAAAGGCAAG GTGACCCACA CTGAGCTTCG GCACGGCACA GCCATTCTGC CAAAGCGCTA 1020 GCACACCACT CAGGCACCCC CTCCTCCCCA GTCCTGCTGC AGGGACAAGG GCAGGCCCCG 1080 GCTCTCCATT TCACCACTCG AGTTCTCGGA GAGGACCCGT GAGTGACTTC AACCCTGGCT 1140 CCCATACCAG CTGCTTCTCA GGAAGACGGG CCTGGGCCGG TTCTCACTTG CCAGTGGGAC 1200 TTCACATAGC CGTTTGTCAG CTCTGTCCCC CAGCGACCGG CCTTTCGAAA TAAGGGAAAG 1260 AAATGTACCC ACTTCCTCCA CCTCCTGCCC CAGAAGGCCT GGCATGCTTG CTGCCATGCC 1320 ACCCGAGTCA CTCGTCACTG GAGCCCAGGG AGGAAGGCCT CATTCACCTG TTTTATAGAT 1380 AAAGAGCCTG CGATGCAGCG TGGCCAGGAG TCCACCCCAG GAGGGCCAGT CGTGGCCAGC 1440 GGTGGGAGGG GCTCTGGGGA GTGGCCTCAC CCTGTGGCCC CAGCGTAGCA AGACACAGTT 1500 CCCAAGCTCA GTTCCCAGTG TCAAGGAGAT CCAGAATTTC AATGCAGTTG GCTTCATCTT 1560 TTTTCCTTCA CCCCCTACTT CGGCCCAGGC TCCCAGGCTT TTCCTGTAAT CAGAGCCCAC 1620 CAGGAAGCAG GAGGGCCCCA GAAGATGACC CCCACAAGCA CCCCAGAGGC CAGGACGGAG 1680 GCTTCTGTGT GGAGGCTCGT CTGCCCCGTG TGTGCACATG GTTTTAGGTA CACACACCCA 1740 GCCCTTTGCA TATCAGGAAG TGTTCAGATG AAAGCAAACA GGCTGGGGCA GAGCGGTGGG 1800 AATGGGGTCA GGAGTGGGAA AGCGAGCATG GAGGGAACGA ATTTCTTCTC CTTCAAGCTG 1860 GCACCTTTGC GAGGCCACCC CGAAGAGCAG AAGGTTTAGC TTCCTCCTAG CTGAGGGGTG 1920 GGGAGGGTGC AGGGGTTCCC AGCTCAGGGA GGAGAGGAGG AAGGGTGTGA TTCTTTCACT 1980 CTGAGGTTTT CTTCTGAGGC TGTGGCTGTG GAGGGTCCTA CTCCTCTTCC TGAGCCCTCC 2040 TACCACAGAC CTGGCCTCCC AGCGAGTTCT TCCTTTGCTC CCTCTGGTCT CTGCTCAAGA 2100 AAGAGCCAAG CAGGGGCCCA GGAGGAGAGA GCTGGGGGAA GGTGGGGAAC CCGCCCCGGG 2160 AGGAGAGAGC TGGGGAAGGG GGGGAACCTG CCCCGGGAGG AGAGAGCTGG GGAAGGGGGG 2220 AACCTGCCCC GGGTGGAGAG AGCTGGGGGA AGTGGGGGAA CCTGCCCCGG GAGGAGAGAG 2280 CTGGGGAAGG GGGGAAACCT GCCCCAGGAG AGAGCTGGGG AATGGGGGAA CCTGCCCCAG 2340 GAGGAGACAG CTGGGGAAGG GGGGAAACCT GCCCCGGGAG AGAGCTGGGG AAGGGGGGAA 2400 CCTGCCCGGG GAGGAGAGAG CCGGGGAAGG GGGGAACCTG CCCCGGGAGG AGACAGCTGG 2460 GGAAGGGGGG AACCTGCGCC AGGCATATCA GGAAGGGGGC CCCTGCCCCA CAGATTCTGC 2520 CTTTGGGGCA TGAGCTGTTA GAAAGGCAGA GCAGGGAGGG GCTCTTGGTC TTGGCCCAGA 2580 GGAAGAGGCT CGTGGGTGGC AGGTGGGATC TAAGGGCTCC GTGTCTGATG GGGACAGGCG 2640 CCACTCCCTC CTTCAGGGAA CGGGTGTGTT GTGGCAGAAA CCACGAAGCC CTAACCTGTC 2700 TCCTCTCCCA GCAATAGAGA AATTAACAGT GTCAACGAAC ACTCAGGCTG TGTTCTAAGA 2760 GCTTTATGTG CCGGACACAG TGGCTCACAT CTGTAATCCC AGCACTTTGG GAGGCCGAGG 2820 CGGGCGGATC ACTTGAGGTC AGGAGTTCAA GACCAGCCTG GCCAACATGG TGAAATCTCA 2880 TCTCTACTAA AAATACAAAA ATTAGCTGGG CGTGGTGGTG GGTGCCTGTA ATCTCAGCTA 2940 CTTGGGAAGC TGACACAGGA GAATGGCTTG AACCCAGGAG GCGGAGGTTA TAATGAGCCG 3000 AGATTGTGCC ACTGCACTCC AGCCTGGGCA ACAGAGCAAG ACTCCGTCTC AAAAAAAAAA 3060 AAAAAAAAAG AACTCTGTGT ATAAATTCCT TTAATCCTCA CAACGACCCC ATGAAAAGCA 3120 TACTATTTGT ATACCCAGTT TGCAGATGGA AAAACTGAGG CACGATAGCT CATTCACCTG 3180 CTGAAAGCCT GGAGCCAGTA CGGCCAGGCA GTCTAGATCC TCTGTCTGAA CTCCTTTCAA 3240 ATACACACCC TGTTAGTAAT GACAACTATG TTCCTTTTTG GACAGCAATT CACGGTTTGG 3300 AAGACGTGTT TCACGAATGT CTGACGGGTT GTCTCTTTGC CTGTCCTCCT TTCTTCCACT 3360 AACAGTTGAG TGTCTTAAGT AACTCAACGC TGTATGAGGT CCCGAAAGCA TCTCCCGATC 3420 TTCTCAACCC CATGGAAAGA GAGAGAAAGA ATGGCATCCC TCTCATCTTC AGATCCAGAA 3480 ATGGAGGCTC AAGGAATTTA TGTAGGGCTT GCCCAAAGCC AGCAGTTTTC TTTTCTTTTT 3540 TTTTTTTTTT GTGATGGAGT CTCACTGTGT CGCCCAGGCT GGAGTGCAGT GGCGCAATCT 3600 CTGCTCACTG CAAGCTCCGC CTCCCAGGTT GACGCCATTC TCCTGCCTCA GCCTCCCGAG 3660 TGGCTGGGAC TACAGGTGCT CGCCACCACG CCCGGCTAAT TTTTTTTGTA CTTTTTTAGT 3720 AGAGACGGGG TTTCACCGTG TTGGCCAAGG ATGGTCTGGA TCTCCTGACC TTGTGATCCG 3780 CCCACCTCAG CCTCCCAAAG TGCTGGGATT ACAGGCTTGA GACACGGCGC CCGGCCAAAG 3840 CCAGCAGTTT TCAAACCCAC AACAGGTGTA AGACACCATG GGCCCGGCAA TTACATATAT 3900 ATACAGGCAC ACAGACAGAC AACAAACCGA AAGTTCCCTC ACTTATCTTT CCCGTGTATG 3960 ATGCATGCTG ACATTTTTTC ATTGGTTTAA AAATGCTGGT TCAACCCACT GTACTGGTTT 4020 CACAACCCAC TGTACTGATT TCACAACCCA AAGCACTGAT GGGCTGAGAG GCACAGTTTG 4080 AGAAACAGTG CAATACGCCT GCTCTTAATG GCAGGGCCAA GTCTTGCCCT AGCTCTGGCC 4140 CCAGACCAGG ACCCTCAGCT ACCTGCCACA CTGCCCCTCA CTTGGAAAAC AGCTCCGTAC 4200 ACACAGATAA ACTCCTGGAG AGATGGGACG TACTCAGCCT GGCGTGTGGC AAAACAGCTG 4260 CACATTCAGA GTTTCACTCT TGTTGCCCCG GCTGGAGTGC AATGGTGCAA ACTCGGCTCA 4320 CTGCAACCTC CACCTCCCGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG 4380 GATTACAGGG GCCCGCCACC ACGCCCAGCT AATTTTTTGT ATTTTTAGTA GAGATGGGGC 4440 TTCACCATGT TGGCCAGGCT GGTCTCGAAC TCCTGACCTC AGGTGATCCA CCCACCTCGG 4500 CCTCCCAAAG TGCTGGGATT ACAGGTGTCA GCCACTGCAC CCAGCCTTTT TTTTTGAGGA 4560 ATTTCACTTC CGTCGTCCAG TCTGGAGTAC AGTGGCGCAC TCTCAGCTCA CTACGACCTT 4620 CGCCCCCAGA TTCAAGCAAT 4640
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