Tag | Content |
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EnhancerAtlas ID | HS184-11101 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr15:43460390-43461470 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr15:43460394-43460415 | GGGAGAGGGAGAGGGAGAGGG | + | 6.44 | ZNF263 | MA0528.1 | chr15:43460392-43460413 | GAGGGAGAGGGAGAGGGAGAG | + | 6.5 |
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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 |
GH15I043168 | chr15 | 43460362 | 43461444 |
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Enhancer Sequence | GAGAGGGAGA GGGAGAGGGA GAGGGGTCTT TTGTTTTCTT TCCTCACTTT TCCCCAAGCA 60 GAAGGAGCCT CTCTCTTTGC TGGCCTGCCT GGATATGTGG GAGAGGTGAC CACAGTTTGT 120 ACCGTTCTGG GTCACACCTG AATTCACCAT AGTACTGGGT CTTGTCCAAG TTCTGTGGTG 180 ACTACTGCTT GGCTACTGCT GATGTTTATT CAAGGCCCAG GGGCTCTTTA GTCAGCAGAT 240 GGTGAATCTT GCCAGGACAT GGTCTTTCTC TTCAACACAG CAGGTTTTCT TCTGGCCCAG 300 GCTGAGTCTA GAAATGCCAT CCAGGAGTGA GGGCCTGGGC TCAGAGGCTT CAGGAATCTG 360 CTTGGTGCTT TATTTTTACT GTGGCTGAGC TGGTACCCAG GTGGCAAAAC AAAGTCCTCT 420 TTACTTTTCT CTCTTGTTTC CACAAGAGGA AGGAGTCTCT CTTTGAGCTG CACTGCCTGG 480 AGAGTTGGGG GATGGGTGAC ACAAGTACTC CCCTGGCCAC CACAACTGGT GTCTCACTGG 540 GTCTTGTGCA CTCCATTTCC ACTGGCTCTG AGCCCAACAT AGTACCCAGA TTTGCCCAAG 600 GACTGCAGTC CTTGTGGCTT GACTGCCTTT CAAGTTTATT CAGGACCCTA GGGCACTTGT 660 TTAGTCAGCT GGTGCTGGAG CTAGCTGGAA CTCAGGTTCC TACCACTGGG GCAGAGGATT 720 GCCCTCTGGC AAGGGCCAGC TTAAATGCTC CCTCTGTGGG TGCTGGCAGA ATTCTGCCCT 780 GTGTTGTGTT CCCCTGTGAC AGCACTGAGT TCCAACGCAA AGTCTCACAG TCATTTTGCT 840 CTCTCCCACA AGTGCACAGA TTATCTCTGC CACAGAATGG GGGAAGGGTG GTGTAGGCAA 900 TGAAGTACTG TGTTGTCTAC GCTTTTTAGT GCCTCTTTCC TTGATATGAT GTTAAAACCA 960 GGTACTGTGA TCACTCATCT GATTTTTGGT TCTTATGAAA GTGCTTTCTT GTGGGGATAG 1020 TTGTTCAATT TGGTGTTCTG AGGGGAAAGG GGTGGATGAT TGCTGGAAGG TTCTATTTGG 1080
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