Tag | Content |
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EnhancerAtlas ID | HS091-10796 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:109990080-109991520 |
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) |
INSM1 | MA0155.1 | chr12:109990743-109990755 | TGCCAGGGGGCA | + | 6.62 | IRF1 | MA0050.2 | chr12:109990318-109990339 | ATTCACTCTCACTTTCACTTT | + | 7.67 | Nr5a2 | MA0505.1 | chr12:109990897-109990912 | GCTGGCCTTGAACCT | - | 7.25 | PRDM1 | MA0508.2 | chr12:109990326-109990336 | TCACTTTCAC | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_05404 | chr12:109990807-109992123 | Brain_Cingulate_Gyrus |
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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 |
GH12I109553 | chr12 | 109990808 | 109992923 |
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Enhancer Sequence | TAGCATGGGC CTGTAATCCC AGCTACTCAG GAGGCTGAGG CAGGAGAATC GCTTGAACCC 60 GGGAGGTGGA GGTTGCAGTG AGCTGAGATC ATGCCATTGC ACTCCAGCCT GGGTGACAGG 120 GTGAGACTCC ATCTCAAAAA AAAAAAAAAA ATAGTTCTCC TCTCCAGGCC TCAGTTTCCT 180 CATTTATAAA ATGGGAGCAA TGATGTCTGA GACCGTGTTC AGCTCTCATT GTCCTGCAAT 240 TCACTCTCAC TTTCACTTTG GCCCTGTGTT CCTGGAGCCA CATCCCCATC TTCTCATCTG 300 ATTGTGCCTG GCCACCTCTG GAGGCCACCT GTCTCCCCCA CCCACTCAGC AAGCCTGAGG 360 GGCCAGAGGT GCTGCCATGC TGTCCTCAGC GTCACCTGGG GATGAGCTTT TAGAACGTGC 420 TTTGAAAAGG GTCAAATATG ATTGAACAAC AATAGCTATT TTTTGGAGCT GCTATCATGT 480 CTGGGGCCTG TGGACTTATT TCTGAACTCT TGGAAATTGG TATTATTATC CTATTATAAA 540 AGATAAAGAG GCTTTGAGTG GTTAAACCAT TTGCTTAAGG AGATGCTGGA AGTGACAAAG 600 ATGGAATCTG AATTCAAATA GTAGTAGTAA TAGCAAACAA CTGTAATAAC AGGAGCTAAT 660 ATTTGCCAGG GGGCAATATT ACTCTTTTAA GTATTACCTC ATTAAACAAT CCCAGTGACC 720 CATGGGGTGG ATGTTATGAT TCCCATTCTA TAGGTGGAGG AGCAAGACCG AGACAGATGG 780 AATGACTTGC CCAGTCACCA AGGCAGGAGG TGACAAAGCT GGCCTTGAAC CTGAGCCTGC 840 CTGGGGCCAG TGCCCAAGCC AGCTGTTTGA CAGTCCTTCC CTGCACCCCA CAACCCTACA 900 AGCATCAAAG GTCACCCAGC AGCCTCTCCC AGCCAGCCCC AAGTGCATCT TCTCACCCTT 960 CCAGGCTGGA GCTATCTGAC CCTGAAACAG GCTGCTGAAG GCAGCCTTGG GAATCCTGAC 1020 TTAGCTCCCG AAGAGGGTCG CATGGGTTCT CTTAGAAAAG GGATTCTTAC CGGGAGGTTC 1080 CATGGACTTC CTATGACTGG ATGCAAACTT GTGAATATGT GTGTGTGCAT TCCAAAGGTG 1140 ACAAACCACA GCTTGAGAAG TTTCTGATTC TGTGGAATGG GAGAACACGA GGGATGTCCC 1200 CAAAGTTTCT AGGTCTCCGC AATCTGCCTG TCCCTGCCTC TGTTGGACTT TAGCACTATC 1260 TTCCAGGAGG ACTCTGAGAG AAGAAAAGCA ATAGGCCAAG GCAAGTTAAA ACTGTGCCGC 1320 CTGCCTCTAG CTGGACTGAC TGCAAAGATG CATTTATTCC AGCTTGTGTC AGTATTGCCA 1380 GAAGATTCTC AGGCCCCGCC AGAGGGGAGG GATGAGCCAC AAATCCTTCC AGGCACTGAT 1440
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