Tag | Content |
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EnhancerAtlas ID | HS184-04253 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:86542960-86544800 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr10:86543709-86543720 | TTTTATGGCTT | - | 6.62 | CTCF | MA0139.1 | chr10:86543227-86543246 | AGGCCAGTAGATGGCACTG | + | 7.07 | NR2F1 | MA0017.2 | chr10:86544647-86544660 | CTTGTGACCTCTG | - | 6 | ZNF263 | MA0528.1 | chr10:86543097-86543118 | TTTTTCCCTTTCCTCTCCTCC | - | 6.25 |
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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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Enhancer Sequence | CACCTTTGGT GATGTTACAA CATTCAGATT TTTCATGGTG CCGGGATTCT TACACTGGTT 60 CCCTCTTCTC TGGAGTCACT GCCACTTCTA ACTTTTGAAA TTATTTTTGT GCATATATAT 120 TGTTTTTCTT TTTTTTTTTT TTCCCTTTCC TCTCCTCCCT AGGGAGTGTG ACTATAGAGT 180 ATGTTTGGTA GGTTCTTTTG ACTTTGCTTC TATAACTCTG TGCACTTCTG GGGGCAGGTT 240 TATATTGGGC TATGTGGTTC AATCCGTAGG CCAGTAGATG GCACTGCAGG TAAGAGCCAA 300 GTGCACCACA AGCAGATGGG TAATTATGGA ATCTTTGCTT AATGTGAGGT GCTTTCTGTT 360 GTTTCAGGTG ATGGGCTAGA CAATGGAGTG CCTGGTGTCC TGAGCTTCCT GTTCAGCAGA 420 GGCAGAGGAC TCTCTGGCTT GGCCACAAAT TCCCCAATGA CAAGAGCAGT CACCAGCCCT 480 AAAGAGGATG GCTGGGGGAA ATGTGCTGAG GTCTCTGTGG GGAGGGGTGT GAGGGGGCCT 540 CACTGGCTCA ATCTCCTAGA TAGGCAGGAA TGCAATCTGT TTCTCTTTCA CATCCCTGTC 600 TCAGGGTTCA TGACTTTCAG TTCAGATGCA CACTGTATCC TATCTCTAGA AATCAATATA 660 GCTGAGAACC TTGGAAAATA AATGCCTGTC CTTGAATCTC TCCATGGGAG TGGTTTTGGG 720 GTAGAACCTC TTCACTCAGC ATGATATAGT TTTATGGCTT ACCTGCTGCA GAAATGCTGC 780 TGCCTTTTAT AGGGAGGGCT TCTGCCTCTT GGCCCATGCA GGTGGTGTTG ATTGGTTGGA 840 TCAGTCCAAC CTCAGGCCCT GAGGGAAGTG GCCAGGTGCC AGCAGTGTTG GAATGGGCTA 900 GGTAGTTCCC CACTTCCCAG GGCCCTAGAT GGCCCATTGG ATGGTGTGTA TGAGTCAGGA 960 AGGGGCTGGA CCAGGGTCAG GTTAGCCCAG AGTTCAGGTG CTGGCTCAGA TGGGGAGGGG 1020 TAGGCTAGTT TCTGGGTCTC TAGCAGAACT CTCAGGCAAA AGTAGGCAAA ATGCTCAGGT 1080 GGTGAGAGAT GTGCCTGAAG GCAGATCACA GGGCTATTGG GGCTGGGCTT TCAGAAGGGC 1140 TGTGGGCTGC ACCTGAAATG TTTAGGCAGG ATCAGGATGG CTGTACTCTG GGCCTTTCAA 1200 TGGGGGAGGG CTGGTCCCCT CAGCTGGACA GTGAAGACTG GCAGCTGTGG GGTGTGTGGT 1260 CCACTCCCAC TTTCCTCCTG CAGATGTAGT GCTGGATTTC ACTGTTAGGG GCACACAAAG 1320 GTGCCAGGCT TCCCCACTCC CTCCCTGCCT GGGGTGGTGA GGCAGAGGCA GTGGTAGCAG 1380 CAACTGTGGA AGAATTGTCA CTGGCTTCTG AGAATTGGGC TCTCAGAAGA ATGCTGAGTA 1440 TCAGCCATAG TGTTCAGACA GGGGTGAGAA GGCTGCATTA GGGGCCTGCC ACTGAAGCCA 1500 GCAAGTCCCA TTTGGTAGGG AGCAATGGAG GTGGGAAGTC ATCGGGTGCA TAGTCTGCTT 1560 GTTGCTCCTC TGCACCTCAG CTACAGTATC TGCACTGGAG GCACTAAGAA AATGCCCTGT 1620 CTCCCTGTTC TCTCCTTGGC CCAGGGATGG CAAGGAAGGA GGCAGCAGTG GCAGTGATTC 1680 CAAAGGGCTT GTGACCTCTG GGAGTTACAA TCTCAGAATA ATGCAGAGCT GCAGCCACAG 1740 TGTTCAGGCA GGGGTGAGGC AGGTGCTCTG GGGTCCCAAG CTGGCAAGGC CCACTTGGCA 1800 GGGAGAAGTG CAGGTGGGGA GTTTAATGAT ACAGTCTAGA 1840
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