Tag | Content |
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EnhancerAtlas ID | HS002-01000 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:203026820-203028300 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:203027356-203027377 | GGAGGAGGTTGGGGAAAGAGG | + | 6.34 | ZNF263 | MA0528.1 | chr1:203027330-203027351 | GGAGGAGGAGGAGGGAGAGCA | + | 8.14 | ZNF263 | MA0528.1 | chr1:203027327-203027348 | TGAGGAGGAGGAGGAGGGAGA | + | 9.05 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 203026998 | 203027585 | chr1 | 203027670 | 203027951 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I203057 | chr1 | 203026643 | 203029528 |
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Enhancer Sequence | CTAATGAAAA GGAAGAAGAG ACAATTCCAG AACAACCTAT TGATAGAGAT GTGCCCAGGG 60 TGCTTGTGGG ACTCAGAACT CGGCTATGGA ATGGTGGGGA CAACAGGGGC GGCCTCCTTT 120 GGTAGCGACA CCTGAGCTAA AGTGTGAGGG CCACATAGGA ATTAGCCGAG CCAGGGAGAC 180 ATCTGTGTGT GGAGGAAGGG GTTGGTCTGG GAAAGGCAAA AGTTTGTGGG TGTGAGAGGT 240 TGGTATGTAC TTATGCATAT TCTGAGTTGA GAAGGAGGAG GGTGGGCGGA GTGGGGAGAT 300 GGGACTGGAC AGCTAGGCTG GGGCCAGCTG TGAGGGCCTT GCAGCATCTG TTTTAGTTTA 360 AGAGTTCCCC TGAGGCAGTG GGAGCATTGA TGAATTTCGT GCAGGGGAGG AACTCATCAA 420 CTAGAATAAA GGAACCTTTG GACCCAAATG CATAATTAGA CCTTTCTGCA GCTCAGGAAG 480 ATGTGAATCA GAAGACAGCT AGCTGGCTGA GGAGGAGGAG GAGGGAGAGC ACGCGAGGAG 540 GAGGTTGGGG AAAGAGGAAG GAGAAAGAGG AATTTGCTGA GACAGGGAGA GGTCTGTGTG 600 TGAAGGAAAG GGGTGGTCTG GGAACGGGGA GGAGGAACAT GGCCACCTCT GCTCAGAATA 660 TGGGAGTGTC AGCCCAGAGA ATGAGGTCCA GCTCCTTCTT CCCCAGTCCA CAGGGGTGAG 720 GGGAGTTGTG GAGCTGGCCA CAGACAGGGG AAGCTGAACG GTTTGATCAG GGGAAGAAGC 780 ATTTTGGGTG AAGCCTTATG ATTTTCGATG CTCTCCACAC ACGTTGGCAC CTAAACCTGA 840 GACAGCACCT CAGATTGGTT TCTGGATTAC CCAAACTTGT TGCCTACTGT GCACTGTGGG 900 GGGGTGACCG GGACTTAAAA GAATTCTAAG ATTCTGCCTC TGGCCACGAA TTCTGAAGGG 960 TTCTAGCATC AATTCAAGGA GATGTTTAGT AGAAGACAGA ACTCTGCATG TTCCCCTTTG 1020 TGGTTTTGTG CAAGTGAATG CACCCAGAGA AGGAGGCTCA GAGACACAGC TCTCAGTGTG 1080 TGGATTTCCA CACCCCTGAC CCAAGCCAGG GTCATCCTTC TCTCTGAGCC TTGTAGCCCA 1140 CTTGTGTTTG GGGCTCTGGG TTTCCTTTGC ACCTTGGCTT GGAGGAAGGA CAGGTTCTGT 1200 CTAGGATTCT AGGGTCGATA ACTTGGGTCC ATCTGGCTGG AAAACACCCC CAAGGCTGAG 1260 GCTCCTGGGG AGACTCTCTG AACTGGGGAT GACCCGCTTG ATGCCATTCT CTGAGACTGC 1320 TTGGATGCAG GGACACTGAG CAGAAGCTCC AGGAATAATG GTCCCGTCAG GCCATGGGTT 1380 GTCCTCTGCC AAGGAGCCTC CTGCTGCTTC TGTTCCCCAC CCCTGATCCA GGCAAGGGAG 1440 GAGAGGCAGA GGGGCTGGCT GACACACACA TCTCTTTCCT 1480
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