Tag | Content |
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EnhancerAtlas ID | HS187-12059 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:16377010-16378120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:16377798-16377816 | GGAAGGGAGCGAGGGAGG | + | 6.13 | EWSR1-FLI1 | MA0149.1 | chr19:16377786-16377804 | GGAAGGGATGCTGGAAGG | + | 6.15 | STAT3 | MA0144.2 | chr19:16377765-16377776 | CTTCTGGGAAG | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I016266 | chr19 | 16377053 | 16377822 |
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Enhancer Sequence | CGTGCTGTTG CTTCATGGTG ACTTGACTGT GATACAAAGA GGCCACCAAC CTGGACAGGG 60 AAACCTGAGC TTTCTGCAAG CTCCCCAGTA ACTCCAGGCC TGACAGGGGC TCACTTCAAT 120 ACCCCCAGCC CCCGTCTATG AAATAAAGGG TGTTTAGGAT CCATCTGGCA ACGGACACCC 180 ACTCGCCCAG GCCAGACCTA GGGAGGGGCA CAGGGACCAA CGAGGCCTCA GTTTCCCTAT 240 CTGTGAAATG GACAGAAAAA GCCCCGCGGC GCATCATAAC AACCCACCAG GTCTATTGTC 300 CAGCCCTGGG GGCCCCCACA TCCCTCTGAG CAGCTTTGGG GTCCCCAATT TCCTTCCCCC 360 AAGCACACAC GCACTGTCCT CTGCCCCTGA CCGCAGCCGG GTCCTGATAC TGTTTTGTTC 420 TCACCCTGCT CTCCTGACCT GGTGCCACCA GTTTGGTGTC TTAAAAAACC ACAACTTAGG 480 GTGCTGTTAT CTGCTATCAG TGGCGGGACG CGGTGGTTTC GGGGCCCCTC CGTGCACTTC 540 TCAGAAGAGC CAGCCATGTC ATCGCAGGGT GCTTGGCACA AAGCAGCTTG TTTATCAGGC 600 CCCCTCATCG CGATCCCTGC TGATAAGGGC CTTCAAGGCG CCCGACAACT TGTTTACGGG 660 CCTTGTTTTC AGAGATTCTC CATTTGATGT ATCCCGGTCT TGCAGCCCAG GGGTCAGGGC 720 ATTGGGGAGG GGGGAAGCAG GGCTGGGTCG AGGGGCTTCT GGGAAGACTT CCTGGAGGAA 780 GGGATGCTGG AAGGGAGCGA GGGAGGGTTA GTTGCAGAAG ATGGGGTAGG CATTGCAGGT 840 GGAAGAACCT GCATGGGCAG AGGTTTGGAG ATAAGAACCT TGTGACAGGC TGGGGGCAGG 900 GGCTCATGCC TATAATCCCA GCACTTTGGG AGGCTGAGGT GGGAGGATCG CTTGAGTCCA 960 GAAGTTCAAG ACCAGCCTGG CCAACATGGC GAAACCCCAT CTCTACAAAG AAAAAAAAAA 1020 AATTAGCCAG GCAGGGTGCG TGCCTATAGT CTCAGCTACT TGGGAGGCTG AGGTGGGAGA 1080 ATTGTTTGCA CTTGACCTTG AGAGGTGGAG 1110
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