Tag | Content |
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EnhancerAtlas ID | HS052-09905 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr12:123425540-123427120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr12:123426134-123426145 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr12:123426134-123426145 | CATGAGTCACC | - | 6.02 |
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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 |
GH12I122942 | chr12 | 123426680 | 123432837 |
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Enhancer Sequence | GACTGGGGAG AGGAGACACG CGTTCCTGTC CCACCGATAC CCGACTCCTG GGACCCACCC 60 CTGCTACTAG AGAGGAGGCA GGTATAGGGA AAGCAAGGAG TTCTGGCGGG GAGATGCAGG 120 AGGCCACCTG ACCACCCACT GGTGCATTAG ATAACGACAG TAAGGGGAGC TGAGGACAGC 180 AGCATCACTA GCACTCTACC GGCCATCCAG CTGAGTGGGT GCCATCATCC CCACAGGAGC 240 AGATGGAAGC GAAGGAACCG GCAGGGGTGT GGCACAGTGG GAATCCAGCC TTGATCTTTC 300 AATTGCGATA GCATAGCTTT TTTTTTTTTT TTTTAAGATG GAGTCTCCCT CTGTCGCCCA 360 GGCTGGAGTG CATTGGTGCA ATCTTGGCTC ACTGCACCCT CCGCCTCCCA AGTCAAGTGA 420 TTCTCCTGCC TCAGCCTCCA GAGTAGCTGG GATTACAGGT ACTCGCCACC ACGCCCAGAT 480 AATATTTGTA TTTTTAGTAG AGACAGGGTT TCACCACACT GGCCAGGCTG GTCTCAAACT 540 CCTGACCTTA AGTGATCCGC CCACCTCACC CTCCCAAAGT GCTGGGATTA CAGGCATGAG 600 TCACCAGACA TGGCTTGATT TCAATTTTCA AAATGGGTCT TAATGTGTAC TATAAATAAA 660 TATATTCTCC TTGGGTAAAA ATACATAGAA TATGAATGTA AATCATAATA ACGGCCCATT 720 TTCTTAAGTA TTCTCTATTT ATTTTTTTTG AGAGGAGGGT CTCACTCTGT TACCCAGGCT 780 GGAGTGCAGT GGTGTGATCT TGCTCACTGC AACTTCTGCC TCCCGGGTTC AAGCAATTCT 840 CCAACCTCAG ACTCCTGAGT AGCTGGGACC ACAGGCATGA GCCACTACTA AGCCCAGTTA 900 ATTTTTTGTA TTTTCAGTAG AAATGGGGTT GCACCATGTT GCCCAGGCTG GTCTCGAACT 960 TCTGAGCTCA AGGAATCCGC CTGCCTCAGC CTCCCAAAGT GCTGGGATTA CAGGTGTGGG 1020 CCACTGCGTC CGGCCAAGCA TGCTCTGTAT GTTAGGAGGT AGGTTCTAAC ATTATCTCCT 1080 TTTTTACTGA TGAGGAATCT CAGGCACAGA GGGCTCAAGT AACTTGGCCC AGGTCACAGA 1140 GCCTAGAAGT GGCAGAGCCA GGATTTGAAT CCAGGCCCAT CTGTCTCCTG AGTTCAGGCT 1200 CTTAGGTGCT GAATGTCCTC ATTGGTGATA AGGGGGTGAT ATCGGCATCT GTGTCCTGTT 1260 ACTGTGAAGA CAACAGCAAC AGCCGGTAGT AAACACCTAA AACCCCAGAG CTGGCCGGGC 1320 ACAGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCG GAGGCAGGCG GATCATTTGA 1380 GGTCAGAAGT TCGAGATCAG CCTGGCCAAC ATGGTGCAAC CCCATTTCTA CTGAAAATAC 1440 AATTTTGTAC TAAATTTTGT ACTAAAAGTA CAAAAATTAG CTGGGCATGG TGGTGCATGC 1500 CTGTAGTCCC AGCTACTGGG GAGGATGAGG CAGGAGAATA GCTTGAACCC GGGAGGCAGG 1560 GGTTGCGGTG AGCCAAGATT 1580
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