Tag | Content |
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EnhancerAtlas ID | HS081-00482 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:44350650-44351650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr1:44351632-44351643 | AAATCACAGCT | + | 6.14 | SREBF1 | MA0595.1 | chr1:44351378-44351388 | ATCACCCCAC | + | 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 |
GH01I043884 | chr1 | 44349837 | 44351801 |
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Enhancer Sequence | CTTGCCAGTC TGTGGATACA GGCTTAATAT TCCAAGCCTT AGAACATGGT TTAGGTTGAT 60 GAGCCAGTGT TGAGGACATT CACCTTATAC GCTGCACCTT AGCCACATTT TTGAGCATTA 120 AGTGAGCTGG AAGATCTCTT AGGAGGGCCC CAGGTTGCCC TTCCTGGCTG GTTAGCCTGA 180 CCCTTATGCT TAATCATAGT CCTCTTTCAG TCTACAGGTC TGCGAGCAGG GCAGCCTCCT 240 GGCTCCTGAG GTTCCATCTA TGCTGTGAGA GACACAGGGG TCAGATCCAC ACTCAGCATG 300 TACTCTCCCA GGGCCCAAAA CCCCCAAACT ACTAGGCTGT AGGATCTAAG GAGAAAGGAT 360 AGGCAAGTTC CAGTGCAACT TCCGTCTCCT CCTTCCCCGG GTCCTTCTCA CGCACTCACA 420 CACACCCTGC TGAAACCTGA TCCTGAGGCT GCCTCGCGTG CCGGGGTGCT GGCGGGGCTG 480 GCGGGCTGGG GCCTGTCTTT TGGAGCCTGC CCCACCCTCC CCTGCTACCC CCTAGGCCAG 540 GGCAAGCAGG TCAGGCGTCC CACACCCCCG CTAGTCTGAC CAGTCATTCT ATACCTTAAG 600 GGCCACCTCC ACCCTGGCCA GGCCCCCAAA CTGGCACACT GGTCTGGACG GAAGCCCCTG 660 GATTCTGTTC CAGGCATAGC CTGAGGTTAG GCCACCTGCA TAATTAACAC ACACACACCA 720 TCTTTACCAT CACCCCACCC CGACATTTCC TGTTGTTTAT AGGCCCCAGC CCATTTTCCA 780 AGGCCTCTGC AGGTGTCAAG CCACCTCACA GGGGATGAAC AAAGTGCAGT GGGAACACTG 840 GAGGAAGAAT GCAAGCCTCC CTCGGGGAGT CAGGGGAGAC TGTCCTGAGG AAGTAGTCTT 900 TCAGCTTGAT AAGAATGAAA CAGAGCAGAG GATGCCAGAG GCTGGGAAGG GAGAAATAGG 960 GAGAGACTTG TCAAATTATA CAAAATCACA GCTAGATAGG 1000
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