Tag | Content |
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EnhancerAtlas ID | HS098-08397 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr10:112123590-112124930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr10:112123797-112123812 | TCAGTGCAAAGTTCA | + | 6.13 | RREB1 | MA0073.1 | chr10:112124312-112124332 | CCCCACCCCACCCCCCACAA | + | 7.38 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_19496 | chr10:112122742-112125490 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_61384 | chr10:112100132-112156157 | HBL1 |
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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 |
GH10I110363 | chr10 | 112123431 | 112124988 |
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Enhancer Sequence | CTGGCTCTTT CAAGACAGTG GAGAATCTGA GGGTGATGAG TTTTGTGGTA TTCAATGGCA 60 GGCTGCTGTG ACAGAGGGCT GCAAATGCCA CTCCGGGGAC ACGTTAATGA AGGCTCTGCA 120 TGCACAACAC GAGAGGCAAT TATTCTGTTC TCCCTGGCAC TGGGTCCTCC TGGCAGGAGA 180 GCTGCCGCCG ACGCAGCTGG AAAGAGTTCA GTGCAAAGTT CACAGAGACA GCCAGATGGA 240 GAATGAACAA GACTTGCCGT GTGGCTCAGC CAATGCCAAA CAGACCAACC GCTCATCTGC 300 AGGCCTTCCC CTGATCCTCG GGAACATATG CAGGAAGGGC ATGGTGGGCG GAAGAGGTGG 360 AGACTTCCGC TGGCAGATGC GAGAGGCATC TGGGGTGCTT CCGGCCTGCG TGTAGGCTGC 420 CATCTCTGAA GCTCCCCGGG CTTAGGGCTG CCTTCCCTTC TGGCCAGGTG TTGTCAACAT 480 AGGATGCGAG GAGTCATCCC AAGACAAAAC ATGGCCAGAC AGGTGAGCCA GAAAAAAGAG 540 GCAGTGAATG CACATCAGTT TGTGGATGAT TTTCCTGGCG CCCATTTCGT AGGCCGACCC 600 GGCCTCTTTC TCTCAGGTTC ACGCAGGGGA AAGGCTCTTC GAGGTGCTGG AAAGAAGACT 660 TTGTCTCCTT CCTTTTCGGC TTGGACCAGC CCTATTAGTG GAGTTTTCTA GGCAAATCTG 720 GTCCCCACCC CACCCCCCAC AAATCAGGTG AAGTCAGGTT AAAAATAATA TTGAAGGCTG 780 CCGTGAGTGC CAGTTGAGTC ACAGCCCTGA GGGTGTGTGG GTTGCAAGTA AGTGGGTCCC 840 ACACGTTTCC CAGGGAGATG ATGGGGCAGA AACAGGTTGT GGAGTCTGCA GAGGGGTAAA 900 ATGAACCCCA GATCTTAGCA GCAGCCTGCC CCCACCCCCA CCTGCTGGCA TTTCCAGGCC 960 AGAAGGGACT GTTCTGTCTC ACTGTTTCTC AAAGGCCACC TGCTGCTGCC TCAGTGAGTC 1020 AGAAGGGCCT GTGTGGCTTG TCGTGGATCA CTTGGAACCT GGCCACATGC CTCCCTTTTC 1080 TATTTCTGTG CCTCAGAAGA TGGCAGTACC ACCCAACACC CCACCCAGAA AATCGCTGCC 1140 ACTAGCTCTA GTGAAGCCTC ATCTCAGGGC TAGTTACCTA GTAAGAAGAG CAGTGCTGAG 1200 AATTCCGGCA GGTAGAGATG AGGTCTGCAG CAAGGGGAAA GAGAGGAGAC TTCTGAGGGC 1260 AGCTGCTCAA TGGAGGAATT AGGGAGGGTT GGAAGCAGAG TTATCCTCAG GATGAGTTAG 1320 CGACAGTCCT GGCAATAGGA 1340
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