Tag | Content |
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EnhancerAtlas ID | HS187-05574 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:32756610-32757880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr12:32757031-32757042 | GATGAGTCACT | - | 6.02 | IRF1 | MA0050.2 | chr12:32757227-32757248 | TGTCCTTTTCACTTTCTCTTT | + | 6.51 | JUN(var.2) | MA0489.1 | chr12:32757032-32757046 | ATGAGTCACTTTTC | - | 6.2 | JUND | MA0491.1 | chr12:32757031-32757042 | GATGAGTCACT | - | 6.32 | Nr5a2 | MA0505.1 | chr12:32757333-32757348 | GCTGGCCTTGAACTC | - | 8.25 | RUNX1 | MA0002.2 | chr12:32756974-32756985 | CTCTGTGGTTT | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 32756660 | 32757167 | chr12 | 32757477 | 32757833 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I032603 | chr12 | 32756656 | 32758861 |
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Enhancer Sequence | GCCTGGCCTT TGTTTCTATA ATGTTTATTA TTTTTTTTTT TTAGAGACAG GGTCTTGCTC 60 TTGTCACCCA GGCTAGAGTG CAGTGGCCCA GTCACAGCTC ACTGCAGCCT TGAACACTTG 120 GGCTTGAGCA ATCCTCCCAC CGCAGCCTCT CAGGTAGCTG GGACTACAGG CATGCGCCAC 180 CACCCTGGCT AAATCTTAGA ATTTTTTTAT AGAAACAAGG TCTGGCTATG TTGCCCAGGC 240 TGGTCTTGAA CACCTAGACT CAGCCTCCCA GAGTGCTGGG ATTACAGGCA TGAGCCACTG 300 CACTCAACCA GTATATGGAG ATCCCCCCCA GCACTTTGAA TATGTCATTC TCCTGCTTTC 360 CGTCCTCTGT GGTTTGAGAT GAGAAGCCAG CCATTGATTG TATTGATACT CCCATGCGTG 420 TGATGAGTCA CTTTTCTCTT GCTGCTTTCA AGATGTTCTC TGTTTTTTGG CTTTCAGCAG 480 TTTAAATATG ATGTGTCTGG GTGTGGACCT TTTTGTATTT GTCCTGGTTA GGGTTGGTTG 540 AGCTTTTTGC ATTTGTAGAT TGATTTTTTT TTAATCATTT TCAGAAGTTT TCAGCCATTA 600 TTTCTTCAAA TATTTTCTGT CCTTTTCACT TTCTCTTTTT TAAAATCTTT TTACTCCCAT 660 TACACAAATT TTGGTGGGTT CCTTTTGTTT GTTTTGGAAA TGGTGTCTTG CTGTGTTGCC 720 TAGGCTGGCC TTGAACTCCT GGGTTCAAAT GATACTCCCA ATCTTTGTTC TATTATTCAG 780 ATTGTATAAT TTCTACTAGT CTTTCTTCAA GTTCCCTGAT TCTTCTGTCA TCTCAAATCT 840 GCTGTTGAAC CTATAGTGAA TTTTTCTTTT CAATTACTGT ATTTTTCACA TCTACAACCA 900 CAACTTCTGG CTAGTAGAGT TATTGGCTCT CACCTCTCAC TCACCTCAGG GATCTTCACT 960 TCTACTGATG TTGTTGGGTG TGTATGTTGC CCACCACTCC AAATGAATGA GCCCTTTTCA 1020 GCCTCAGCAG AGGAGCTGCC AGTCCTCACA GTCCGTGCCA CCCTGATGGC CCCTTCATAG 1080 TGACTGAGCT GGGAGAGGAA CAGGAGCAGC CACAGGCTAG AATGCCACAG ATTCTCACCG 1140 TTCTTACCCA AAGTTCAACA ATTTTTAAAG TGTAAACAGA TTTCAGGTTG TTGCATGCCT 1200 TTTAATCAAT TTCTAAAATG CAAATATTGT TTTGTCAATT TTATCTAGCT TTATAGCTGC 1260 TTTTTTTTTT 1270
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