Tag | Content |
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EnhancerAtlas ID | HS187-09352 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr16:30141640-30142660 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF9 | MA0653.1 | chr16:30142440-30142455 | AGTTTCACTTTTGTT | - | 6.15 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I030130 | chr16 | 30141521 | 30142810 |
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Enhancer Sequence | CCCAGCTACA GGACTGAGGC AGGAGAATTC CTTGAGCCTA GGATTTTTGT TTTGTTTTGT 60 TTTTTTGAGA CAGAATCTCG CTCTGTCGCC CAGGCTGGAG TGCAGTGGTA AGATCTCTCA 120 GCTCACTGCA AGCTCCACCT CCCAGGTTCA CGCTATTCTC CTGCCTCAGT CTCCCGAGTA 180 GCTGGGATTA CAGACGCCTG CCACCACGCC CGGCTAATGT TTTGTATTTG TAGTAGAGAC 240 GGGGTTTCAC CGTGTTAGCC AGGATGGTCT CGGTCTCCTG ACCTCATGAT CCGCCTGCTT 300 TGGCCTCCCA AAGTGCTGGT ATTACAGGCG TGAGCCACCG CGCCTGGCAT GAGCCTAGGA 360 GTTCAAGGCT GCAGTGAGCT GTGATTGTGC CACTGCACTT CAGCCTGAGC GATAGAGCAA 420 GACCTACAAA AAACAAACAA AACCCAAAAC AGAATCACAT GTAACACACA GCTGTGGACT 480 GATTGGTTGA CAAAAGTGTG GTGATCAGAG GCTGGCAGGA ACTTCACCAT GTATTTCCGC 540 TAGAAGCAAT GTTCAGTATT CTCTAATTCA TTGTTTGTGG TGACTTTGGG GAATATAACC 600 ACCACAGAGA CAAGAATCAA CTTTGAATGT GTCATCCCAC CACCTGCTGG CTTCCGTTGT 660 TTCTGATGAG AAATCAACTG TCAATCTCAT TGGAGTTTCC TTGTACGCGA TGAGTTGTTT 720 TTCTCTTGCT GCTGCCAAGA GTCTCTTTTT GTCTTGTTTG TTTATTTATT TATTTATCTA 780 ATTTATTTAT TTTGAGATGG AGTTTCACTT TTGTTGCCCA GGCTGAGTGC AATGGCACAA 840 TCTCAACTCA CTGCAACCTC TGCCTCCCGG GTTCAAGCAA TTCTCCTGCC TCAGCCTCCT 900 GAGTAGCCAG GACTACAGGT GTGCGCCACC ATGCCCAGCT AATATTTGTA TTTTTTTTTT 960 TAAATTTTTT GAGATGGAGT CTCACTCTGT CCCCCAGGCT AGAGTGCAGT GGCGTGATCG 1020
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