Tag | Content |
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EnhancerAtlas ID | HS037-05054 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr10:86073300-86074250 |
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) |
ELF5 | MA0136.2 | chr10:86073576-86073587 | TACTTCCTGGT | - | 6.02 | FOSL1 | MA0477.1 | chr10:86073726-86073737 | AGTGACTCATC | + | 6.02 | JUND | MA0491.1 | chr10:86073726-86073737 | AGTGACTCATC | + | 6.32 | Nr2f6(var.2) | MA0728.1 | chr10:86073346-86073361 | GAGGTCAGGAGTTCA | + | 6.22 | PLAG1 | MA0163.1 | chr10:86074093-86074107 | GGGGCTTTAGGGGG | + | 6.19 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH10I084313 | chr10 | 86072914 | 86074536 |
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Enhancer Sequence | GCCTGTAATC CCAGCACTTT GGGAGGACGA GGCGGGCGGA TCACTTGAGG TCAGGAGTTC 60 AAGATCAGCC TGGCCAACAT GGTGAAACCC CGTCTCTACT AAAAATACAA AAATCAGCCA 120 GGCGTGGTGG TGGGCACATG TAATCCCAGC TACTCGGGAG GCTGAGGAAG GAGAATTGCT 180 TGAACCTGGG AGGCGGAGGT TGCAGTGTGC TGACACTGAC CCACTGCACT CCAGCCTGGG 240 TGACAGAGTG AGACTCTGTC TCAAAAAAAA CAAAGATACT TCCTGGTAGT TTCCCACCTC 300 ATTACGCATA TACTTACTGC ATTTGTTTTA AGAGACACTT GGAATTCCAC GTTTTATTGT 360 GGGGTATAAA AATGAAGCCC GCATATTGCT GCTTTAACAA GTAGCCTTCT GTCCACCTTC 420 AAGAATAGTG ACTCATCTGG AAGGAATGGA GGCATTTCCT CTCTCATCAA TAGAAGTAGA 480 GATTGGTCTT TGTGTTTCTG AAGACTGGTG GGTGCTCCTT AACTTAGAGC GAAGACACTT 540 TTTTCATCGT TAACAGTTAG AGCTCCTTTT TGAGAAGCGT TACCTGAGAG GATGTTAAGC 600 CTTATTATGA GAGAAAGGAG GCAAAATGAG TGTTTGCAGG AGTGGTACTA GAGAGATTTG 660 GAGCTGGCAC CCTAAGACAT GACTGGGAGT AGGGAACAGG GCCAAGGTCT CTGGGTCCTG 720 AGGCTGGGAA CCTGGCCATT GATGAATGGT CCCATCGGTG GTGTGTGGCC TGGAATAGAT 780 CTGAATGGAG GAAGGGGCTT TAGGGGGTTC TGGACAAATG CCCAGGAGGG ATATCAGACC 840 AGAGAAGGGG CGCCCTGCAC CAAGAGGCAA CTCAGCAGGG CAGGCCCAGT GGTGGGAAAG 900 GAGTCTACAG CGGTGGTCAT GTCCCCTGTC TGCCCTGCCC AGTGTGGGGA 950
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