Tag | Content |
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EnhancerAtlas ID | HS092-12683 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:78281900-78283330 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr12:78282541-78282552 | CATGAGTCACT | - | 6.14 | JUN(var.2) | MA0489.1 | chr12:78282594-78282608 | GAGAGGTGAGTCAT | + | 6 |
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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 |
GH12I077888 | chr12 | 78282481 | 78282650 |
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Enhancer Sequence | TGCAAAAGAT TTAGGAAGGT TATTTAAATG TACATTTTAA ACCCATACTC TAACTAAAGT 60 GGTTATCATT GTATACAATT ATCCAAATAG GCCAAGCATG GTGGCTCATG CCTGTAATCC 120 CAAGGAGGTA GAGGCAGGGG GATTACTTGA GACCAGGAGT TTGAGACTCA ACTGAGACCC 180 CCATCTCTAC AAAGAAATAA ATAAAAATTA GCCTGACATA GTAGCATGTG ACTATAGTCC 240 CAGCTACTGG GGAGGTTGAA GCAGGAGGAT TGTTTTGGCC TAGGAGGTCA AGACTGCAGT 300 GAGCCGCGAT CATGTCACTG CACTCCAGCC TGGACAGCAC AGCAAGACCC TGTTTTAAAA 360 ATTAACCAAT TAAATAATTA AATAATTTCT GCAGTGAGCT TAATGGCTGA TTTTGTTTTT 420 GAAATACTTT ATCTTAATAC AGTAAGACAA AGTAATGAAG AGAAGCATAA GTTAATAGCC 480 TCATTAAGTT TTGCCCTCAA ATGTTATGTC CCAAGTAAGT CTTTGGGTTG GAGTCAATTC 540 CTGGTTGAAT TATCTAATAT GTATCCAAAG ATCCTATAGT TTATGCTGAT TAAGAATGAC 600 CTGTATGTAT TAAGCATTGT GTATGTGGGA TGTGGAATTG GCATGAGTCA CTGAATGTTC 660 TAAGTCTTCA AATGTTTTTA TCTTTGTTTT CTCAGAGAGG TGAGTCATAT GTGTGTGACT 720 GTGGATAGGA CCGGTGTTCT TCTGCTCAAT AACATACATA CTCAGGGGGA ACTCCATCTT 780 GTTCTATATA ATATGGACAA GTGATTTCTT GAAAAAAATT TTAGGACAGA TTTGGTCAAT 840 TGAGTGTTTT AATCTCAGAA TAACCTCAAT GCCCTCCAAA CCTGCATCTG CTGGGCCCAG 900 CATGATGGTT AGCATCCACC TTTTGTGTGG TGCAATGGTT TATTTTATGT GTCAACTTGA 960 CTGGACAATG GAGTGCCAAG ACTTTTGGTC AAACATTATT TTGGGTGTGT ATATGAAGGC 1020 GTCTGGATGA GATTAACATT TAAATCAGTA GACTGAATAA AGCAGATTGC CCTCCCTATT 1080 ATTGGTGGGC CTCATCCAAT CAATTGAAGA TCCAAGTAAA ACAAAAATGC TGATTAAGAG 1140 GGAACTTTAC CTGCCTGACT ACTTGAGCTG AGACATCAGT CTTCTGTCCT GGGACTGCAG 1200 CTTGCACCAT CAGCTCTCCT GCTTCTCATG CTCTCAGACT TGGACTGGAA CTACACCACC 1260 ATCTTTCCTG AGTCTCTAGC TTGCTGGCTA CAGATCTTGG GCCTTTTCAG CCTTCATAAT 1320 TAGTTCTGTT TCTCTCGCAA ACCATGAGTA ATATAGGTAG ACATATCTAT GGCTGAAATA 1380 CTGGACAATT AATGGAAATG TGACTATTTT AACTACTCTA AGTTAATTCA 1430
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