Tag | Content |
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EnhancerAtlas ID | HS116-20901 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr20:33170640-33172050 |
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 | chr20:33170858-33170873 | GCAGGTCAAAGGTCA | + | 7.16 | Nr2f6 | MA0677.1 | chr20:33170859-33170873 | CAGGTCAAAGGTCA | + | 7.73 | PPARG | MA0066.1 | chr20:33170865-33170885 | AAAGGTCAGGGTGACTCAAT | + | 6.26 | Rxra | MA0512.2 | chr20:33170859-33170873 | CAGGTCAAAGGTCA | + | 7.58 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr20 | 33170652 | 33171022 | chr20 | 33171562 | 33171703 | chr20 | 33171368 | 33171418 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I034582 | chr20 | 33170781 | 33170950 |
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Enhancer Sequence | ACTTCCAAGC TCTGGTCAGG AGAGAGTTGG GGGACAGAGC TCAATCTCGG TGCCCCTCCG 60 AGAGCTGACC AAGTGCTAAA GGGAAGCCAA CAGGGAGAGG CTGGATCTAT ACCCTCCTCA 120 GCTACATTTC AACCACATGC ACATGGCCTA CTTCTGCACA GTACCTAGAT GCCTAGCCCA 180 TGAAGGTTTT CTTCAGAGAT TAATGACCTT TTTGTCTTGC AGGTCAAAGG TCAGGGTGAC 240 TCAATGGGTA TGAATCTGAG ATGTGCAGAC AAACATGTCC ACACCCAGAA TGCTCCAGTG 300 CTGCTGTGCA GCAAGTGCCT CAGAAACGCA GCTTGGCAAA GGCGTGCAGC CCTGTAGCCT 360 CTAAGAAGCG TCCAGCTATA GCTCAGTGTG AACATCTTCC TAAACACAAT CCACATCACT 420 GGCTTCAGGC TTTTCAGGTA GCTGGTAACA ACGGCAACAT TTCTATGAAA AGGCTGGTGA 480 AAATGCGGTG ACAAAAAAAC AGACTACAGC CTCCTGCAGC ACTGCACAGG GACTGGGGTG 540 GCCTGAAGGG CCCTGTTCCT ACAAAGCTGG CACTGGAAAC AAATCTTGCA GGGGGCAGGA 600 GAGCTTAGGT AGAGCTTCAT ACCCAGGCAG AAGAGAAGAC AGCAGGGAGA GCAGGTCTCT 660 TCATATTTTC TGTCCCCACA ACTGTGTGGG CCTGGCTTAG GTCATAAAAT GGTGACATTA 720 TTGCCTAGCC AGGAGCAATG TGTGGCTTTG CATGCAGACA ATAAAAGCTG CCGGAGAGCT 780 GGCTGCACGG CCAGTGCGGA AAGGTGCCCT GGGATCCCTG CTCCTCTTCA CCCCATGGCT 840 GGGCCTAACC GGAACAAGGA CAGGGAAGGT GGACCACAGA CAGCTGGAGA GCTCAGCTGG 900 GCAAGGCTGC CAGAGTTCCG GAGCCTGCCA GGCCATGGAA GGAGGGTGTT CTGTCAGAAG 960 CCAGGCCAAG GCTGTGTCAT GGGAAGGAAG CATCAGCTTT TGAGATTTTA CAGAATGGGA 1020 ACCACGTGCA TTGGTGCACA GACCATGGAG AATGGCAGGA AGGTTAGGAC AGAGAACTTG 1080 AGCTCTTGAA ACCTAAATCA AACTCTTTCA GGTTCCCCAG ACCATCTAGG CGTATCTGTA 1140 CCTGTCTGTG TCTGTTTTCC CTTATCTGAA GCTAGGATAA TAGAACCATT TCCGGAGGCT 1200 ACTAAAAGCA ATCTCTCCGG AGCTTGGCAT GGTGCAGGGG GATAAGCATA GATTCTGGAG 1260 CCAGACAAAC CTGAGTCTAA ATCCCAGCTC CACTGCTTAC TAGCTGTGTG ACTGGGAAAA 1320 TCATCCCACC TCTCTGAGCA TCGATTTCCT CAACTATAAA ATGGGAGTGA TAAGAATCTA 1380 ACGCCTACCT CCAGGAGTTG CTAGGTTAGG 1410
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