| Tag | Content |
|---|
EnhancerAtlas ID | HS184-18026 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr20:32495890-32496730 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SRF | MA0083.3 | chr20:32496285-32496301 | TGGCCATAGATGGGCA | + | 6.19 |
| | | 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 |
| GH20I033907 | chr20 | 32495609 | 32498650 |
| Enhancer Sequence | CCAGGAAATA CTTTAGACCC TCTCACCTCA TTCCCACTTC ATCCCTTTGG ATCCAACTAC 60
TGATAAGACT TCGTGCCCCT GATCTCCTGT TTCCTGCAGG AGCTGGGGGC AGGGCCCACC 120
TTTCCCAGCC CTTTGGGTTT GACCCATGGA GGAGCTTTGG GAGTAAACGT CCGGCGGATG 180
AGCCACAGTT GGTGGAGCGG GCACTGTTGG AGCTCTACCC AGCTGCCCTC GGATCCTCTT 240
AGCATTTCTG TTTGCCCAGG TTCCAGGTGT TTTCATCTGA CAGCTTCCAT GTGAGATTTT 300
TCTTCAGAGG ATTGCCCTTG GGCTCCTGGA GCCACTGGCT GCACAGCACA AGGACCTGGA 360
AGTGCCTGCA GTTTACTTCC CCGCCGGGTG GCCCTTGGCC ATAGATGGGC AGATACACAA 420
GAGCATGAGT CCAGCTCCTT TGCCTCCAGG CACAAACCGA GCTGTAATTT ACATTCCTCG 480
GCTCCCAGTG GGATCAGATT GAGGCTGGGA CGCTATCTGC TAGTGCACTC TTGCTTGGCT 540
TTTTCTCTTT CCTATCTTCT TCCCCCACTC CTGCCAGTTT CTCCTAGGAG CACTTCATAA 600
ATCACTTGCC CAGGAATCGT TGTCTTTGGT TTGCTGCTAA GCCAGTCCCC CTGTCCTGGG 660
GATCAGCAGG CTATGGCAAA AGTAATGCCC AGAGGAAAAG CAGGCTGTGA GTGTGCAGCA 720
CTTTTGCTAG CTCATGCTTG GGAGGGCCTG GACCAGCATC CTTGCATGCC CTAAATCAAC 780
AATGCTCCAG ACTTGCAGGT GGTCTGATTT TCAATAGGAA AGTATAACCT ATTTTTTATT 840
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