Tag | Content |
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EnhancerAtlas ID | HS076-05058 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:203518070-203518910 |
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) |
HNF4G | MA0484.1 | chr1:203518727-203518742 | ACAGGACAAAGGCCA | + | 6.03 | RREB1 | MA0073.1 | chr1:203518607-203518627 | GGGGTGGGGGTGGGGTGGAG | - | 6.62 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_00433 | chr1:203513781-203518813 | Adipose_Nuclei | SE_40925 | chr1:203517827-203518906 | Left_Ventricle | SE_46073 | chr1:203517538-203518872 | Osteoblasts | SE_55853 | chr1:203516457-203518914 | u87 | SE_67709 | chr1:203516457-203518914 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I203549 | chr1 | 203518348 | 203519397 |
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Enhancer Sequence | AGAATAAATG TAGGAAAGAA TCTAATTCTC CAGAACTTCA GAGCCAAAAG GGGCCTCGGG 60 GATCAGCTGA CAAACCCCTT AGTAACAGAA CCTTCCCAGC AGCCTTTATT TCCCCACATC 120 TCTCTTACAT TTTGCCAAAG ATAATATTCA CTTTGATGTT GCAAAAGCTT TAGTTTGCTT 180 GTTGTGTTTC CTCTCTCCAT AATGGTATGT TAGGCCATCC TTTTGTATTG GCAAATTGGT 240 CTGACAAAAA GAGCATTATA AATTGTGAAA ATACAAACAA ATTCTCCCAG CTCTGAAATT 300 CTCCTTGGAC TTCAGTGGTT GACACAAATA ATTTAGAGGT GATGGAGTTC CTTGAGTGCA 360 GAGGGTGACA GAAGTTCATT CTTCCTCTGG CAAAGAGAGA GAGAGAGAGC TGTCTCCCTG 420 CAGTTTGGGA GACTGGGCAA CCACTCTCTA GGGATGCTAC AGAGCTTGCT GTCCTCCCTC 480 CTTCCAGACA GGTTGGCAGT CCTGCTGAAA GCTGACTCCT CTTTCCTGAA AGTCTATGGG 540 GTGGGGGTGG GGTGGAGGAG TGCTATGCAT CCAGGTGCCC CGCTCTGGTG TAACCTGAGA 600 CTAGAAGGCA ACTATATTCC AGGCTTTTGA GAATACTGAG TCAGGGTAAT GGGGATGACA 660 GGACAAAGGC CAGGCAGGAC ATGCTGGAAT TTGTTTTTGT TTTGTTTTGT TTTTTGAGAC 720 AGAGTTTCAC TCTTGTTGCC CAGGCTGGAG TGCAGTGGCG CTATCTCAGC TCACTGCAAC 780 CTCCACCTCC CGGGTTCAAG TGATTCTTCT GCCTCGGCTT CCCAGGTAGC TGGGATTACA 840
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