| Tag | Content |
|---|
EnhancerAtlas ID | HS053-37967 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr8:6719910-6720970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr8:6720292-6720309 | GGGTTCACGGTGACCTG | + | 6.36 |
| | | 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 |
| GH08I006863 | chr8 | 6720881 | 6726933 |
| Enhancer Sequence | CAAAACCACC TTATGAGAGA TGGAGGCAGA TGGAGGCAGC CAAGGAAACC ATGTGTGGAT 60
GGGCCAGTCA GGCTCCTTCA CGCTGGCCGG CTGGACGAGG TGACTCAGGT GTCCCATCCA 120
TGACACCTCC AAGAGCAAGA TGGAGAATGA GGAAGGAGAC TGAGATGAGC TGAGTTCTGA 180
TTGTATGTCA GGGGCTGGCT GGGCTGGATG AGTGCCACAT AAAGGTTATC TCACTGAGTC 240
CTCACACCTG TCCGGGGGGG TCCATTTATT CTACTCACTT TCATACACCC AAGAATGCAA 300
GAATCAGAGA AGTTGTGCAG CTTGTCCAAA GGCCCAGGTC TGTCTGACTT GAGAGTCAGC 360
CTGTGGTTTC CTGCCCCACG TGGGGTTCAC GGTGACCTGC TTTGGTGCTG GGTCATAGTC 420
GCTGGATGAG AGATTCTCTA GTAGCTGGAG GAAGGGGATC TAAGGGGGGC TGGGCTCACA 480
GAACATGGGG AGGTGAGGAA AAACACACTA GAAGCTCTGG CTCAGGTGGA GGCAGGAACG 540
CTCTGGGGTG AAATGTGTTG TCAACCATGG GATGACGGCT GCCCCGGGAC AGGACATGTC 600
TAATCACACT CTGCCCTGGT TTCTGCAAGA GTCACTGGGC TGGTTACGAA GCTATTGTTT 660
CTCAGCCCCA AGTTCCCTAC TCAGTACCTG CTTTGCGGTG GGGCGGATCT GGGAAGGTCC 720
TGCTCAGCTC TGCCCACAGG GCAGGGAGCG GGTAGGGAGG CTGGTGGGGA GTGGGGGAGG 780
CTGGTGGGGA GTGGGGGAGG CTAGAAGGGA CGTGGGGAAG CTGGTGGGGA AAAGGGAGGC 840
TTACGGAGAG TGGGGAGCCT GGCAGGGAGT AGGGGAAGCT GGTGGAAGAG GGGAGGCTGG 900
CGGGGAGTGG AAAAGCTGGC GGGGAGTAGG GAGGCTGATA GGGAGTGGGG AGGCTGGCGT 960
GGAGGTGGGG ATGCTGGCAG GGAGTGGAGA GGCTGGAGGG GATGGGGGAG TCTGGCAGAG 1020
AGTGGGGGAG GCTGGCAGGG AGTGGGAGAG GCTGGAGGGA 1060
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