Tag | Content |
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EnhancerAtlas ID | HS184-02962 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:236562770-236563810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr1:236562783-236562794 | GGCCACACCCT | + | 6.32 | ZNF263 | MA0528.1 | chr1:236563398-236563419 | TTTTCCCTTCTCTGCTCCTTC | - | 6.23 | ZNF263 | MA0528.1 | chr1:236563419-236563440 | TGCCCTTTCTCTTTCTCCTCC | - | 6.44 |
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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 |
GH01I236398 | chr1 | 236561905 | 236563735 |
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Enhancer Sequence | GCCACCACGC CCTGGCCACA CCCTGGCCAT GAGTTAATTT TAAGTGACTT TTTACATTGA 60 GAAAATTCAC AAGACTGTCA CAGTCACATG GAAGGAAAAC AATGATGGTG GTTATAGTGT 120 AGCTATCACC CTGTGTCTCT CCCACTGAGA AACAGTCTCA CAATGGATGA GCCAGATTTG 180 TCTGTCAAAT GTTTGTAAAA TCTGTTTGTT CATGATTGTT CATACAGATA GATTTTACAG 240 ACAGAAACAA ACAACCGGGC TTTGAAGGTC TGGGTCAAAG GTGGCACAAT TCCTTGCTTC 300 GTTGCAGTAA GGCAAGTGCC GACGGCCACA GAGCATTGCA AAAGAGCACA TTCTCCCTTT 360 GTTCTGAGAC TCCACACCGC AGGGCTGTTT CCTGGGGGAA CCCTGGGCCT GGGCCACCAA 420 CTCAGGACAG CCCCAGTGGT GGCATTCACC TCTCACTGCC CCTCCTGTGG GCTTCAATGG 480 GTCCAAGGTG GCAACCTACC CTCCTGTGGC ATTGGGCGCA GTACCCAGGA CTAAAGGATA 540 AACCACTTCC TGGAGCACTC ATATGTGCAA AGCTGGACCA GCCAATTCTT TCTGCAGATA 600 CACCAAAGAG AGGGATGGCA ATCTGTGGTT TTCCCTTCTC TGCTCCTTCT GCCCTTTCTC 660 TTTCTCCTCC ACGTGGGTTT TCCCAATGCT CACTTCATTT CTCTTCCTTT CTTACAACGC 720 CTCTGCTTTG TGAGTTTCCT TCTCTCTACC CAAGCATTTT CCCTGAGCTT TATCTCTTTG 780 TTTGCTGTCT TCCCTCATCC TCCCCTGCCC TCTTCTGTTT GATCCCCCGT CAGTAGCCTG 840 GCTGACACAC TTAATGCTCG GCTGCCCTCC AGAGAGGTTG CTGTAGGGAT GTACTTCTGT 900 GATCCTTGCC CCTTTCCCAG CTTGTTCAGC CCCTGCTGCG GGGTCTGAGG TTGACAGAGT 960 AGCCGAGGTC AGGGTGAGGT GCTGAAAAGA CAGAGGAAGC TCAATGAAAC AGTGTCAGCA 1020 CCACCACGCA GCAGCACCCC 1040
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