| Tag | Content |
|---|
EnhancerAtlas ID | HS184-26334 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr6:44443160-44444180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:44443599-44443618 | CGGCCAGCAGGTGTCACTG | + | 6.87 |
| | | 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 |
| GH06I044475 | chr6 | 44443335 | 44444192 |
| Enhancer Sequence | AAAGAGAAAA TGAAGATTCT GAGAAAGTGA CTGTTCTTAG AATCAAGAAG TGTTATGGGG 60
GAAACGATGT GTTCTTGGAG CATTTAGGGG AGGAAATAGG TAAATCCAGG AGAGGGTGCT 120
TGCCACTGCA AGCTGGTCTA GCTCCCTGCA CCCTCAGCTC TGTCCAGGAA CCCTCTTCCT 180
CCAAGTTCTT GAAGGCTGTG CGGGGCCCAG GCTCCAAAGA GGACAGATGC AGAGGCCACT 240
TGTCCTCCCC TCCCCAAGGA CCCAGAGCCC GCAGCTCCAG CAGCATCTCC AGCCAGCTGC 300
CTGTCTGTAG CCGACGCCCC CCAGGGCTGC AGGGTTGGGC GAACTGGCCT CTCCTGTGCG 360
GCTGACCAGG TCCCCCGAGC TTCCTTAGGG TTGCAGGCAA GGAGGCTCCC GCAGGGAATC 420
TGGAGCAAGG TGCATCCGGC GGCCAGCAGG TGTCACTGCT GCCCCAGAGA CGGCCGGCCA 480
CGGGCTGTGG CGACACGGTG AGCTGGAACA AACCGCTTTG TTCCTGCTTC ACAGGCTTTA 540
CCTTACAGCA GGGTTAGGAG CCTGTTTACC TGCACTTCTG CCCAAGGAAA GGAGTAAAAG 600
CCCTTCTCCT CCTTCCCTCC AGAGGACCCC ATGGAGGCCT GCTGGGCTGC GCCCCCCTCA 660
CTGGCCTGGC CAGGGCGTGT GGGAGCACCC AGCAGCTGGG GCTCCTGGGC ACCCACTGCC 720
TGCCGGGCTT TGCCCTGGGA GCTGTGGGGC CCACAGCCCT ATGGACTTCA TACTTCTGCA 780
GGGGCATGGG GCAACTTGAA GGGGTGTTGG TAGGTGTTAC AAAGCGAGGC CCAGCCTGGG 840
TCTGGCACGG TGAATCCTCC TTCCTGGCCG CCTCTCCTCA CTCCGAAGGC TTCGCGGATG 900
GTCTTGCTCC AGGTTGTCAG TTGCTCCTCT GAGTGGTGGG TGAAGAGGAA GCGGCTCCCG 960
TGTGTGGGGC TGTAGGCGGA CCAGCTGTTC TAGTTTGCTC ATCACTGAGG AGTTCCTGGA 1020
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