Tag | Content |
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EnhancerAtlas ID | HS184-14429 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:80309460-80310370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:80309868-80309887 | TGACCACCAGGGGGTGCTA | + | 7.82 | ZNF263 | MA0528.1 | chr17:80309708-80309729 | GGAGGAGGAGGGTCGGGAGGC | + | 7 |
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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 |
GH17I082351 | chr17 | 80309676 | 80310277 |
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Enhancer Sequence | ACACCCCTGC ACACTCGTGA GGGCATGCTC TCACACACAA ACATGCACTC GCAATAGGCC 60 TCCAGGGCTG GGGCCGGCCG TGGAGCTGGA CCGAGGGAGG GAGCTTGCTG GGGTGGCCCA 120 GGTATAGCCC CTGGCCCGGC CTCAGCCCAC CCGGCAGACT CTCAGCTGAA GGAGGACGCG 180 GGTTGCCGTC GGGATGCCGT GTGCAACATC CCAACTCCAC AGATCAGAAG ATGGAGGCAG 240 AGCCGATTGG AGGAGGAGGG TCGGGAGGCC TCAGGAATTG CTAAAGGGCC AGCCATGGTT 300 CTCAGTTCTT CCCAGCAACC AGTCCAGAGA CCAGGCCAAT GGCAGGGCCC CTTTGCGGGC 360 TTGGCTGATT TGATGGTACA AAAGCACGAG CGTCCGTGCA GACTGAAGTG ACCACCAGGG 420 GGTGCTATTG GCACACAGCA AGTTGGCGCC CAAATCCAGA GCCTAGAAAT TGATCCTGCT 480 GCCTCCGGGC TGCTCTGCCG CACCCACAGG TGCCCAGGGA TGCCAGGCGC CTGCCCCAAG 540 CCATGTGGGG GTGGCACAGG TGCACCCGGA AGCCCCCAGT TTCCATAATC TTCCCTCCCT 600 GCCAGGAGGC GTGTGGGTTC GCCAAGTCCT GCTTCCAGTG CCTGCTTCTC CAGTCTCAGA 660 TCTCAGCGAG CACACCAGGG GTATGGGAGG CCTCACACCC AGGGGCTGTT GCAGCCACGC 720 CGCTTCCTGT GTGTGGGCGC TGTGCATGGC AGGGTGGACA CGACACCACC TCCCAGTTGT 780 CATGGGCAGA GCCCCTTTCC TTGGACAGAA CCCCTGGTGC CCACCCCTAG GAGGTAGGAT 840 CCAGACCAGT GGGCAGAGGA GGGGGAGGCC ATGCTCCTTT GGGGCCATTT GTGTGCCTGG 900 CGGTGGCCCC 910
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