Tag | Content |
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EnhancerAtlas ID | HS049-03582 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr17:80309280-80310420 |
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 | CGAGGCGTCT GCTGGAAGGA GTCTCTGAGG TCACCAACCA CGCCGGGCTG GGGCCCTGCG 60 ACCGAGGCAT CTGCGGGAAG GAGTCTCTGA GGTCACTCCT GCCCACAGGT GCACGTCTGT 120 GCACCCGCCC ACTCCTGCAT ACACACGAAC ACACCTGTGC ATGTATACAC CGCACCCCAC 180 ACACCCCTGC ACACTCGTGA GGGCATGCTC TCACACACAA ACATGCACTC GCAATAGGCC 240 TCCAGGGCTG GGGCCGGCCG TGGAGCTGGA CCGAGGGAGG GAGCTTGCTG GGGTGGCCCA 300 GGTATAGCCC CTGGCCCGGC CTCAGCCCAC CCGGCAGACT CTCAGCTGAA GGAGGACGCG 360 GGTTGCCGTC GGGATGCCGT GTGCAACATC CCAACTCCAC AGATCAGAAG ATGGAGGCAG 420 AGCCGATTGG AGGAGGAGGG TCGGGAGGCC TCAGGAATTG CTAAAGGGCC AGCCATGGTT 480 CTCAGTTCTT CCCAGCAACC AGTCCAGAGA CCAGGCCAAT GGCAGGGCCC CTTTGCGGGC 540 TTGGCTGATT TGATGGTACA AAAGCACGAG CGTCCGTGCA GACTGAAGTG ACCACCAGGG 600 GGTGCTATTG GCACACAGCA AGTTGGCGCC CAAATCCAGA GCCTAGAAAT TGATCCTGCT 660 GCCTCCGGGC TGCTCTGCCG CACCCACAGG TGCCCAGGGA TGCCAGGCGC CTGCCCCAAG 720 CCATGTGGGG GTGGCACAGG TGCACCCGGA AGCCCCCAGT TTCCATAATC TTCCCTCCCT 780 GCCAGGAGGC GTGTGGGTTC GCCAAGTCCT GCTTCCAGTG CCTGCTTCTC CAGTCTCAGA 840 TCTCAGCGAG CACACCAGGG GTATGGGAGG CCTCACACCC AGGGGCTGTT GCAGCCACGC 900 CGCTTCCTGT GTGTGGGCGC TGTGCATGGC AGGGTGGACA CGACACCACC TCCCAGTTGT 960 CATGGGCAGA GCCCCTTTCC TTGGACAGAA CCCCTGGTGC CCACCCCTAG GAGGTAGGAT 1020 CCAGACCAGT GGGCAGAGGA GGGGGAGGCC ATGCTCCTTT GGGGCCATTT GTGTGCCTGG 1080 CGGTGGCCCC CATTGTGTCC CCAAGTGGGG TTTATGGTGT TGCCGAGGGC TGTGGGGGGC 1140
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