Tag | Content |
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EnhancerAtlas ID | HS062-12782 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr5:7815900-7816880 |
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 | ATGAGGAAAT TGTTACCCTC CATATTAGTT TGCTAAGGCT GCCATAACAA AGTACTGCAA 60 ACGGGGGACT TAAACCACAG AAGTTAATTG CCTCGCTGTT CTGGAGACTG GAAACCAAAG 120 ATCAAGTCGT CAGCAAGGTT GGTCTCTCCT GAGGCCTCTC TTCTCCCCCT GTCGGGCCTC 180 TTTCCTTCCT CTCCTTGTGT CTTCACACGG CCTTCCCTTT GTGGGTGACT GGGTCCTAAC 240 TGCCTCTTCT TAAAAGGACA CCAGTCATAT TGGATTAGGG CCCACCCTTA TAAGCTCATT 300 TTATCTTAAT CACCCCTTTA AAGACCCTAT CTCCAAATAT GGTCATATCC TGAGAGACTG 360 GGGTTAGGAC TTTAACATAT GAACTTGGAG GGACACAATT TAGCCTAAAA TCCTCCATTT 420 CAAGGCCTAA GAGGGCAAAA GGAGGGGGAT GTTCCCAGAA CTAGAGAGAG CTGCAGTGCA 480 GAGACAGTAG CTGCCACCCG GGGCAGTAGC CCTTGTCCTC CGTGAAGAAG ACTGACCCCT 540 GTGGAAAGCC TGCGGTGAGC AGGGAAGAGG AGGAACGAGG CCCCAAGCCT CCTCCCTGCT 600 CTCTTTTTCC ACTGCACCTC CCACTGGGCA ATCGCCACTG GCAGCCCAAG GACAAGGAGC 660 GGGCACCCCC TAGCGGTCAG GCCACCAGAG CCAGAGCCCC GCAGAGAAAG GCAAAGGCCG 720 GCTGTGGAGG GGAAAGGAGG GAAGAAGGCG CCAGCCCCTC CTCAAAGCCA GCTTCCCTTG 780 GTGATTTCTG GACTAATACG ATACAGGTTC CCCGTGGTCA GCCTTAGCCC GCATGATGCG 840 TTTGGCCTGA GGGGGCCTGA GACACGGAAG TCAGTGTCTT CTAGCACCTA ACGTCTCCCC 900 TTGGCCACAC AGTGCTTCCT TGAGATGGGA TTTGATTCTT ATAGAATGTT TGCAGTGCCT 960 TGTAGCATTA GAATTTGCCT 980
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