Tag | Content |
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EnhancerAtlas ID | HS052-17405 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr18:21364240-21365640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr18:21364821-21364842 | GGAGGAGAAAGAGGAGAAGAT | + | 6.72 | ZNF263 | MA0528.1 | chr18:21364818-21364839 | AAGGGAGGAGAAAGAGGAGAA | + | 6.73 |
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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 |
GH18I023784 | chr18 | 21364297 | 21365804 |
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Enhancer Sequence | CTTATATATG GATGTTACAT GTGATGGTCC TACCTGGACC TTGTCACTTC CCTTCTTTCC 60 AACCTTACCC TGCCTCCTCC CTGGTAGTTA AGCACATGGA CTCTGAAATA ATCTGTTTGG 120 GTTCAAATCC TGGCTCTGGA GAGGAGGTGG TATCTGAACA GCATTTAGGA ACCTGCCACC 180 ACTTCTCAGA TCCTGTTGGG GCGGGTCTCC AGATGCCAGT TGGGTTTGCA AATTGGAAGT 240 GTGTGAATAA GATTAGAAAG ATGGGAAGGT GGATGACAGA AGGAGGCAGG GTGTTCTAGA 300 GAGAGGGGAC AGCACATGCA AACCATAGAG ACATGAGACC ACAAACCCCC TCCTCCCCAC 360 TTGTTTGTAT CCTAGTATCC CATCCCGGCA AGGGTCGCTG AAGGGGGGAT GGAAGGTGGG 420 AGGAGGAAGT GTCTGGTCCG GTCCCTAGAG CATGGCAGGT ATGCACTCAA TGCTGGGTGA 480 GTGAACACAT GAATGAATGA ATTTGCCCAA ATTATTCTCC CCTGCCTCCT TTCTACTGTC 540 TGACATTATT CTTCTTTCTG CAGACAATGG TGTAGGGGAA GGGAGGAGAA AGAGGAGAAG 600 ATTATCAGTC CAGGATCAAG GCAGGAAATA AAACACCACT TCAGACACTA TAAAAAGAAA 660 GAGATTTATT ATAGGTAATT AGGTGCTAGC CCAGAGGAGT TGTTAAGAGC CAGAGCAGCA 720 GGCTCTAGGC TGGGCTTCCA AGGAGGCCTC CAATGGAATG GCTGGGTTTT AAGCCCAGAC 780 TGCTATGTCC CAGTGCAAGG ATGGGAAGCC CATGGTTGGT GACTTCATCT CTTGGCATCC 840 AGGAAGCCAG AGTCAGAGCA CAGCTGCATA AATGCTCAGC CAGCTACAGG ATGCAGCCTC 900 CTCCTTATTT CCCATCGGTC TAATCTTATT CACACACTTC CAATTTGCAA ACCCAATTGG 960 CATCCAGAGC CCTGCCCCAA CAGAGTCTGA GAAGTGCTGT CTTTAGCTTT CCAGCCTCTG 1020 AACACTGGAG GATATTAGAA TAGGTATTAG GTCATCTCAC CTGCAAGGTC AGCCACACTA 1080 AGGAACTGTA AGCATGAAAA ACTCCCTCCC CTAAGCTGGA GGACAAGGTA GTGAAGAGCA 1140 GGGGTGGCAC TAGCTATCAA CTTGGGCAAG TTACTTAACC CCTCTGTTCC TCAGTTTCCA 1200 AAAAATAGTG CCTGTCTCAT AATTCATTGT TGTGAGGGTT ACATATGTAC TGACAGGTAA 1260 AGCTCTTAGA ACTGAGGAAG TAATTGTTCA TAAGTTAGCT ATTCACTTGC ACCTTTCTTC 1320 TCCTGACCTA TACTTCCCTC TGCATCATTT TAAGAGCTTG TAGTCCCATT TCCAGCCATC 1380 TCCCTGTTTG TTTAAATGCC 1400
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