Tag | Content |
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EnhancerAtlas ID | HS046-10009 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr13:45885010-45886230 |
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) |
ZNF263 | MA0528.1 | chr13:45885633-45885654 | GGAGGAGGAGGAGGAGGAGGA | + | 12.34 | ZNF263 | MA0528.1 | chr13:45885729-45885750 | GGTGGAGGGGAAGGTAGAAAG | + | 6.11 | ZNF263 | MA0528.1 | chr13:45885642-45885663 | GGAGGAGGAGGAAATGGATAA | + | 6.81 | ZNF263 | MA0528.1 | chr13:45885627-45885648 | GGTTGAGGAGGAGGAGGAGGA | + | 7.72 | ZNF263 | MA0528.1 | chr13:45885639-45885660 | GGAGGAGGAGGAGGAAATGGA | + | 8.04 | ZNF263 | MA0528.1 | chr13:45885636-45885657 | GGAGGAGGAGGAGGAGGAAAT | + | 8.61 | ZNF263 | MA0528.1 | chr13:45885630-45885651 | TGAGGAGGAGGAGGAGGAGGA | + | 9.8 |
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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 |
GH13I045311 | chr13 | 45884659 | 45886335 |
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Enhancer Sequence | AATTTGGAAG CAAGACTGCC TCTCTTTCCA CTTAGCCAGC AGGAATTTCA ATAATAAGAT 60 GCGGCAGCAT CCATTGACTT TGTACCACCT GTCTTTTATT GTAAGTGTTC ACCCTAACGG 120 TTTTTATTAA CGCTTTGGCT TCCGTCGCTA AGCAACGTGC CACGTTGGGG CTCTTCGCCA 180 GACTACACCT GTACAAATGT CAGCCTCATT CTCCTGGCTC TGAAGGAAAC GTGACCGTTC 240 CCCAAACATG CTCTTTATGG TTGCTTCCTC CTGTTCTTTT TCTCCTTCCC TGAACCGCTC 300 CCAATAGAGA CAGGTTGGCG CTTCAGTGCA TCTCAGATCC TCTGGCGCCC GGGCGCCCCC 360 TCCCGGCGAC ACCTCCCGGC TGTGAGCGCG CGGGAAGAGG CCAGAGGCAG GGCCTCTCAC 420 CTGCTCGGAC TGCAAACCAC AAAGCGTCTC TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT 480 TTTGAGGGGC GGAGGTGGTC ATTTTTATGT TCCCTGGGCA AAGCGAGCAG CCGTTTGGCT 540 TATAAAATAG CAACGACTGC AGTGGCCCAC ACTGTCATCA CGAAATGCCG CCTCTTGTCA 600 TGGTCCCCGG AAAACAGGGT TGAGGAGGAG GAGGAGGAGG AGGAAATGGA TAATGCCGAT 660 GAGTTACTTT TTTTTTTTTT TAATTTGGGT ATGTTCGAGT ACATTCTGGT CTGAATGGCG 720 GTGGAGGGGA AGGTAGAAAG GAGGCGTCTG CCGAGCAGCA TCCGCGCGGA GCGAGCTGCG 780 GTCCTCGGGA CCCCGCAGCA GGAGCCACGA GCCCGCCCCG GCGTCCGAGC CCTGCAGGCG 840 AGGCCAGGCT TGGCGCGGAG GGACCTCAGC GTCCGGGGAG CGCTCGCTGT CTTTGAGTTC 900 CTGCTGCCAG AGCCGGGCCT CCTCTGCTCT CCGCAGCCTC GCAGGGAGGG CGCAGGGGCG 960 AGTCCTGGGC GGGCAGGGCA GCCGCGCCCG CCAGAGAGAC AAAGGCCAGG GGGTCTCTGG 1020 CCGCAGCACT TTCCAGCGCC GCCCGGTCCT CACACAGAAA ACTCTTCTAG CTCTGCGGGT 1080 GCGGCTCTAA ACGGTAATGT TTGCATTTTC TCTAGGGTGA TCCGCAGAGG GGGCCAAGCC 1140 ATAAGTCCCC TCCAAAAGTC TATATGTGTT CATCGCATGT TTACCAGAAG ATTTGACACT 1200 ACACCAAAAA GCACACAGAC 1220
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