Tag | Content |
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EnhancerAtlas ID | HS184-11077 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr15:41953040-41954580 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr15:41953984-41953996 | TGCCTGGGGGCG | + | 6.14 | TCF3 | MA0522.2 | chr15:41953400-41953410 | AGCAGGTGTT | - | 6.02 |
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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 | CCCTCGCGTG TGTGGGGTGC CGCTCCGCGT GGTACGGTCC GCGTGACGAC TTCTCGCCCG 60 GCGCCGGGCT CTAGGTCGAG AGCCACGCTT ACGCGCTTTT CAGTTTAGAG CCTAGGTCTC 120 GTGGTTCTAG AACTCCAAGG GAAACGGTGT CGGCGTCGCT TTTCTGAGAA CTTGGCGCAG 180 CGTTTTGACA CCTGTGCAAA CGTCTTTTCT AACAAGTAAT TTCCGGCCAA ATTGTTTGAG 240 GCAGGACGTC AAGTTTAATA AAGGAGGGCG AGGAAGTGAG CTGTAGGAGT GGGGACTTGG 300 TAAACAAAGG ACCGGTGGTG TGTAAGTGCA GAAATGAGGG AGGGGAAAAC AGGTGGGAAG 360 AGCAGGTGTT ATTTTCTTTA TTCCTCTGTG GGGCAGCCTT TTACCTAGTT CTGTTTATGG 420 GGTTTCCCGT TTCTGTTAAA TGGTCAAGTA GGTCTCTGCC CTCAGTGCAA GGTATCTGGG 480 ACATTAACAT CACCCCCCCA CCGCCCCCCC AAAGCTCCAG TAGCCAAAGT TGAGGGATCT 540 ATGTGTCAGA AGAATATGGG GAAACTAGGG ATCGTTTCAG ACTGGGTCGG GAGTGCAAAA 600 GTGGTAGTGT CTTGCTGTAC AGATTTTTGC CTTGCCTTTC GAACCCTGGG AATGCCTTCT 660 TTCTCTGGCC GGGGTGGAAG CAGGAACGGG TAAATGAGGT CTGAAAGGAG GGGTTACTGA 720 TGGCAGACCA ACACGAGAAA CCAAAGTGCA CTCTTTTATT GGGAAGATAA CTTTCCCAAG 780 GTTCGCCTCG CCGGAGCAAA CACGTGGATC ATGAGAAGTC TCGAGCCCAC CCGCGCGTGT 840 TGTTGTAGAG CTTGCCAGGC TTATGCGGCT GAGTCCCTGG TTAACAACTG CTTGCTCTGT 900 TCGTTCTTTT TGGGCACGAT GCCGCGGCTA GGCTGCAGGG AAAGTGCCTG GGGGCGGCGT 960 GACGGCTGCT GGGAAGGGGG TTGGCAGGGG AGGGTCTGGT GGCTGGTTCT GTAGTCTCCA 1020 AGGTAACAGA ACGCGGCTGG GTCCCGCAGA GCGATCATCG GGTTCCGGCC GGCGGCACGT 1080 GATCTGTCGG GACTCTTCCC CGGAAGAGCT TTCCTTGCGG CATTTTTTCA CGTGGTTCTT 1140 GGCCAGCTGT CCTTTGCAGT TGAAAAGCGG CGGTTTGTGG GTCATTAATA GTCGACGGCG 1200 TCTGCTCCTC TCGGGGAAGG CAGTGAGACC GAGCCTTTTA CTTTCCTGCG TATCGGAACA 1260 GCGCTAGTGT TTCTTGCCGC CAACGGTTGT TTCTAGCGTT TGTGTGGGTT AAGTGGGTTG 1320 GGTCCACTTT ACAGAAAACA CAGGCTAAAG ACTTGAGGAA ATTCAGTGCC CTGGGTACCT 1380 TGGCATACTT ACTTCAAGTT TGACTACTGC CAGTTTCTGC CTTAAAAGTT CTTCAAATTC 1440 TGCTTACCCA ACTGCTAGAG ACCTGTCAGC TTTCTGGCCC TGAGTTGTAG TTAGGGTCCA 1500 TTCTTAGGAA TAAAAAATAC TCCTGCGGCT AGCAGTAACA 1540
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