Tag | Content |
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EnhancerAtlas ID | HS041-08757 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr17:44189400-44190480 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr17:44189516-44189531 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 44189785 | 44189850 | chr17 | 44189588 | 44189638 |
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Enhancer Sequence | TATATTATTG TACACCTCTA TAGGGAGTGT TATATAATCA TTAAGAATGA AGACAGGCAC 60 GGTGGCTCAC ACCTATAATC CCAGGGCTTT GGGAGCCCAA GGTGGGTGGA TTGCCTGAGG 120 TCAGGAGTTC AAGACCAGCC TGACCAACAT GGTGAAACCC CATCTCTACT AAAAAATAAA 180 AAAATTAGCC AGGCATGATG GGGTGCACCT GTAGTCCTAG CTACTCAGGA GGCTGAGGTA 240 AGAAAATCGC TTGAACCCAG GAGGTGAAGG TTGCAGTGAG CCAAGATCAA GTCATTGCAC 300 TCCAGCCTGG GTGAAAAGAG TGAAACTCTG TCTCAAAAAA AAAAAAAAAA AAAAAAAAAA 360 AGAATCCAGA CCGGGAGTGG TGGCTCACGC TTGTAATCTC AGCCCTTTGG GAGGCTGAGG 420 CGAGCGGATC ACCTGAGGTC AGGAATTCGA GACCGGCGTG GCCAACATGG TGAAACCCCA 480 TCTCTACTAA AAATACAAAA ATTAGCCGGA CATGGTGGTG TGTGCCTGTA GTATCAGCTA 540 CTCAGGAGGC TGAGGTGGGA GAATCGCTTG AACCTGGGAG GCAGAGGTTG TAGTGAGCCA 600 AGATCACACT ACTGCATTCC ATCCTGGGTG AGAGTGAGAC ATTGTCTCCA AAAAACAAAA 660 CAAAACAAAA CAAAAAACTG GGCAGATAAA TTTTTTTTTT TTTTGAGATG GAGTGTCACT 720 CTTGTTGCCC AGGCTGGAGT GCAATGGCAC AATCTTGGCT CACTACAACC TCCGCCTCCC 780 AAGTTCAAGT GATTCTCCTG CCTTAGCCTC TCGAGTAGGT GGGATTACAG GCATGCGCCA 840 TCACGCCGGG CTAATTTTGT ATTTTTGGTA GAGACAGGGT TTCTCCATGT TGGTCAGGGT 900 GGTCTTGAAC TCCCGACCTC AGGTGACCCG CCCACCTTGG CCTCCCAAAG TGTTGGGATT 960 ACAGGCGTGA GCCACCAGGC CCGGCCGGGA CAGATAATTT TAGACATCAA TTTAAGTGGG 1020 AAGAAGACTA CAAAGAATAC AAAGAAACTA GCAATGCCTG AAGACATTTT TTGTTGTCAC 1080
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