Tag | Content |
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EnhancerAtlas ID | HS139-42854 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr5:7815730-7816760 |
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) |
RUNX1 | MA0002.2 | chr5:7815971-7815982 | AAACCACAGAA | - | 6.32 | SRF | MA0083.3 | chr5:7816229-7816245 | TCTCCAAATATGGTCA | + | 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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| Number: 1 | ID | Chromosome | Start | End |
GH05I007815 | chr5 | 7815832 | 7816970 |
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Enhancer Sequence | ACAAATTCAT GTTAAATATA AACAGGTAAC AGGAATGATA AACAGAAATT AATAGGAAAT 60 CTGCATAGAA ATGTTCACTT CTTCCCACTG GGAAATCTTC AGGACTTCTC TCCTTCAGCT 120 CTGTAATTCC CTCCTCCTCG TGGGATGACA CAGCCCTCAA GGACGAGTAA ATGAGGAAAT 180 TGTTACCCTC CATATTAGTT TGCTAAGGCT GCCATAACAA AGTACTGCAA ACGGGGGACT 240 TAAACCACAG AAGTTAATTG CCTCGCTGTT CTGGAGACTG GAAACCAAAG ATCAAGTCGT 300 CAGCAAGGTT GGTCTCTCCT GAGGCCTCTC TTCTCCCCCT GTCGGGCCTC TTTCCTTCCT 360 CTCCTTGTGT CTTCACACGG CCTTCCCTTT GTGGGTGACT GGGTCCTAAC TGCCTCTTCT 420 TAAAAGGACA CCAGTCATAT TGGATTAGGG CCCACCCTTA TAAGCTCATT TTATCTTAAT 480 CACCCCTTTA AAGACCCTAT CTCCAAATAT GGTCATATCC TGAGAGACTG GGGTTAGGAC 540 TTTAACATAT GAACTTGGAG GGACACAATT TAGCCTAAAA TCCTCCATTT CAAGGCCTAA 600 GAGGGCAAAA GGAGGGGGAT GTTCCCAGAA CTAGAGAGAG CTGCAGTGCA GAGACAGTAG 660 CTGCCACCCG GGGCAGTAGC CCTTGTCCTC CGTGAAGAAG ACTGACCCCT GTGGAAAGCC 720 TGCGGTGAGC AGGGAAGAGG AGGAACGAGG CCCCAAGCCT CCTCCCTGCT CTCTTTTTCC 780 ACTGCACCTC CCACTGGGCA ATCGCCACTG GCAGCCCAAG GACAAGGAGC GGGCACCCCC 840 TAGCGGTCAG GCCACCAGAG CCAGAGCCCC GCAGAGAAAG GCAAAGGCCG GCTGTGGAGG 900 GGAAAGGAGG GAAGAAGGCG CCAGCCCCTC CTCAAAGCCA GCTTCCCTTG GTGATTTCTG 960 GACTAATACG ATACAGGTTC CCCGTGGTCA GCCTTAGCCC GCATGATGCG TTTGGCCTGA 1020 GGGGGCCTGA 1030
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