Tag | Content |
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EnhancerAtlas ID | HS118-19009 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr9:15279170-15281300 |
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) |
GLI2 | MA0734.2 | chr9:15281201-15281216 | CACTGTGTGTGGTCT | - | 6.12 | GLI2 | MA0734.2 | chr9:15279714-15279729 | GGACCACACACAATG | + | 6.41 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29496 | chr9:15275587-15279702 | Fetal_Intestine_Large |
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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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Enhancer Sequence | GAAAGTCTCT GGTGTAGACC AGGGATGAGC AAAAAGAAAC CTCCTGCATG ATCTTGCTCC 60 ACCCTTGAAC TATCCAGCTG TAACAGAAAA TTGGCAGAGT TAGCAGTCCT TTACTTGTAG 120 CTCTGCTCCA AAATAAATGT CTCAAAAAGA GAACACAGAA CCTTATCCAC TCAATATGAG 180 TGTTCGGAAG AGGCAGTTCC CAAAGAGTAA GGCTTCAAAG ATGATCTCAA ACTGAGAAAT 240 CCTATAATGG GGGAGAGAGA AGGTAAAGGG ACTTGAGCTC ACAAGCTTAG AACCACTCTA 300 TCTGGGTTCA AATCCCAGTT TCACCACCCA CTGGCTCTGT GACCTTGAGC AAGCTATTTT 360 CCTTAGGACC TCAATTTCCC ATGTCACTCA GCTGTCCATA GATTAATGTC AGATGTGAAA 420 AGCACTTAGA ACAATGCATC CAGTAGAAAG ATGAGTTATT ATCACTATTA TTGTTGTGCC 480 TTGAATCTCC TAAAGGTACT CGTGAGTGGC ACTGTGTGCT GCAGCCTGGG AAAGGTTAGG 540 AAGTGGACCA CACACAATGC TTGGCACTAA GAATCCTAAG TCACCTTCTC TGTGGCTGAC 600 ATGTCCTGAT GTCCCCAAAT AGATCAGTCT ATTACTATTG GTGTCAGGAA ACTACAAACA 660 GGGCCAAATT CCACCTGCTG CCTTTTCTTT TTTTGTAAAT AAAGTACTTT TTTTCTTTTC 720 TTTTTTTTTT TTTTTTTTTT TGAGACGGAG TCTCACTCTG TCACCCAGGC TGGGGTGCAG 780 TGGCATGATC TTGGCTCAGT GCAACCTCCA CCCCCCGGGT TCAAGCGATT CTCCTGCCTC 840 AGCCTCCCAA GTAGCTGGGA CTACAAGTAC ATGCCACCAA ACCCGGCTAA TTTTTTTGTA 900 TTTTTAGTAG AGACAGGGTT TTGCCATGTT GGCCTGGCTG ATCTTGAACT CCTGGCCTCA 960 AGTAATCGGC CCACCTTGGC CTCCCAAAGT GCTGGGATTA CAGGTGTGAG CCACCGTGCC 1020 CGGCCTGTAA ATAAAGTGCT ATTGAAACAC AGCCACAACT CAATCAATTG ACATATTGTC 1080 TAAGGCTGCT TTCCTGTAAC AGTCACAAAC TGCATAGCTG CAACTGAGAT CACAGAGTCC 1140 TCAAAGCCAA AAATATTTAC GCTGTCCCTT TACAGAAAAA GTTTGCCTAC GTTTGCGCAA 1200 TGAATGAAAC ATCAGGTTTC CTTCCCTACC GCATTGGATG CTTTGAGGAT AGAGTGAGAA 1260 ACAAATGTTA AAAATCTATA AAGTTCAAAG GGTTGGCAAA TACGAGAAAT TATTTAGCCC 1320 AAAAAACTCA CTGCCTTCAA GATTTAAATT CAAGGGAGAA ATAACACTAA GAACAAAGAC 1380 TGCAGAGTCC CGCTATCAGC TCCATCACTT ACCAACTATG TGTGGCCCGA ACAGTGATGA 1440 TGATACCCCG CTTTTGCTTA GCTGAGACCA CCAAGCAGCC TCCTGGCCCT TGGTATGGTT 1500 GCTGCAGCTA GCTGGCGGAA AAGGGGCCAG CAGGGGAGTT TGCTAGAAGA GGGTCAGGAG 1560 AGGCAGTGGG TATCCCTAAA AGTTAATATA TTGAGAACTT AGCTTGAGTC TGGTCCTTCC 1620 CAATTCCAAA AGTAGGAGGA GTAAAGAATG CGAATGCTTG CAGTGGGGTT TAGTAGAATG 1680 CCTCTCTCAG GGCTCCCCCT ACCATTCTAG AGAGTCGAGG CACCAGCCAT TCTTGCCAGT 1740 CTCATCACAG TGCTTCCCAA AGAGGCTGTT TTGTGTGTTG AAAAGATGAA AACAATGCAA 1800 TTATCCCAAA CAGTATTGAG AAGAATAATT TATTTCTTTT TTCTTTCTTT TTTGTCTTTT 1860 TTTTTGTTTA AATCATCAGT CCCTATTCTG GAAGAGGTAC ATCCCAGCAT CTAGCCCAGA 1920 TGTCCTTTTA TGCAATAGTT ATTTTAACAA ACTTTCTTTA TTTCCTTCCT TTTCTCTTTC 1980 TAAACTAAAA GGAAAAAAAA TCTAAAAACA ACAACAACAA CAACAAAAAC CCACTGTGTG 2040 TGGTCTTGGG CAAGGTACTT CTCTAAGATT CTTATTCATC ACCTGTAAAA TGGGAATAAC 2100 AGTGCCATCA AACTCATGGG GTTGAAGAAT 2130
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