Tag | Content |
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EnhancerAtlas ID | HS089-05694 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr17:29389920-29390800 |
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) |
NR2C2 | MA0504.1 | chr17:29390625-29390640 | TGACCTTTCACCTGG | - | 6.39 | Nr2f6(var.2) | MA0728.1 | chr17:29390699-29390714 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6 | MA0677.1 | chr17:29390625-29390639 | TGACCTTTCACCTG | - | 6.17 | Rxra | MA0512.2 | chr17:29390625-29390639 | TGACCTTTCACCTG | - | 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 |
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Enhancer Sequence | CCCAGGAGGC TGAGGCAGGA GAATCTCTGG AACCCAGGAG GCAGAGGCTA CAGTGAGCTG 60 AGATTGCGCC ACTGCACCCC AGCCTGGGTG ACAGGGCAAG ACTCCATCTC AAAAAAAAAA 120 AAAAAAGAAT CCATGTGCAT TGGAAGGATC TGGCCAAGGC ATGCTGGTAG GTTTTTTCCT 180 GCTCAAAGAT GATTATCTTG TATTCTGCTC CTTGGGCCCC TGTCTCTATT GGTTTTTGGC 240 CCATATAGTT CTCTCTCTCT CTCTCTCTCT CTCTCTCTCT CTCTCTCTCT TTCTCTCTCT 300 GTGTGTGTGT GTTTGATGGC AAATTTCAAA TATACAGTAC ATTATTATCA ATCATAGTCC 360 CCATACTGTA CAGCTTATCC CTATCGTCAT TCTTCACCTT CTAATAATGT TTGTTGCTTC 420 TTACATATTT TGAAGCCTCA TAGAAACTTG AAACTATTTA ATTCAAAGTG GCCTCTTAGT 480 CTCTTTTCTG CTTACGATAA TCGGAGTGGT TTTCTGCTGC TTGCAACCAA CAATTGACTA 540 TATAGACATG TTTGGGAGGC ATAATATAAT GCTGATTTTT TAGGTGTTGT AGGGATACCA 600 AGATGAATGC AGTCTGGAAT GCACTACACA CAGCGCATGA GAATACGGGC TCCGTAGTGA 660 GACAGGCTTC AGTTCACCTC TTGCCTCTGC CACTTACTAG CTGGGTGACC TTTCACCTGG 720 TCTTTTATCA TTGCTGGGTT TCATTTCCTC GTCTGTAAAA TGGAGTTACT AAATGGTCTT 780 GAACTCCTGA CCTCAGGTGA TCCACCCGCC TCAGCCTCCC AAAGTGCTGG GATTACAGGC 840 GTGAGCCACC GCTCCTGGCC TTGATAATGA TTCTTAACTT 880
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