Tag | Content |
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EnhancerAtlas ID | HS043-04529 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:245750430-245752040 |
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) |
Nkx2-5(var.2) | MA0503.1 | chr1:245750929-245750940 | CTTGAGTGCTT | - | 6.02 | YY1 | MA0095.2 | chr1:245751877-245751889 | CAAGATGGCAGC | + | 6.32 |
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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 |
GH01I245587 | chr1 | 245751114 | 245751532 |
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Enhancer Sequence | ACCTTGGCCA TGCTGCCCAC TCACCTAGAG CGCACAGCTG ACACTGAGTC CTCTTCTGAA 60 CCTCATCCAT GAACATATTT ATGAAATCTT TCCTGGCCCC AAGTGGAAAT GCCCCCTCAT 120 TTGGGTCCTC ACTGAACCCC AGTACACAAC TCTTTTGTAC TACTCTATTA TGCTGGGGTG 180 TTTTTTTATT GTCTCACCTG ATAAACCGTA AGCCCCTTGA AGACAGCAAC TCGTTTTTAA 240 GCTCTTTATA ACCCCAGAGC CTCGCACAGT ACCTGGACCA GATTAAGGGG TACTTAACAG 300 ATGCTTAGTG AAGGAAGGAA TGGATTTCTC ACCTGGTTGC TTATCTTCTA GACTCATTTG 360 GGGAGTGGCC AGGAGTCCGG GAGAGCTGCC GGCCATTGTT CCGTCCCGTC TGTATCCCTT 420 GGGCTAGTTT CTTCTAGACT GAGGTTTCTA AGTCCAAACA AGATGAACTG TGCACAGTGC 480 CTCAATTAGG GAACAGCAGC TTGAGTGCTT TGGAAATACA AAAGTGTAGT TTGTAGGTTC 540 ACCTTGAAGG CAAGATCAGA CAGCTCTACG TAAGCCAGAG CTCTGAAACA AAGCTTCAGG 600 CTGGGACCAC TTTGCAGTCT CAGTGCCTGG TAGTGGGGAC TGTTCTACAG AGCCGTGATC 660 AAACCTCCAA CTGCATTCTG GTCTTGGAGG AAAGCTGATT CCGTATGAAG AGAAAAGGCC 720 TGGTGAGAGT ATTTGCAGGG CTGAAGAAAA GTTAACATCT ATAGTTTGGC AAGCAGCAGC 780 TGCAAAGCAT CCGTCCCAGC ACATGATAAA TGCTTCTGAC GTTTCCTTCA GACACAGTGT 840 GCTAGGAAGG CTTTTAAGTT CTCAAATGCA GGAGTCTGCC TTATTGATCA GGTGCCTTTC 900 ATTAAAGGTT TCCAAGCCCC TCGGCTACAG AGGAAACGCT CCCCTCAGCC TCCTCCACAG 960 CCCCAGCCTT TCATGCAGAG GGGATTATCA TTGTTGGAAT ACGGCATATA CTTTAATTTG 1020 GTGAGGCTTT TTGTTTAATG CTTATGATAT GCACACTGGA ACAGACTGGG ATTAGGTAAT 1080 TTTCACATTG AGTTGGTACT TCCCTCCCTA ACCCCCATCT GATCTTCCAT ATACACATTT 1140 TAAGAAGAAA ATAAAGAGAA GACACGTCCT CCTAATGATC CTCCGTATTA GAACTTACCA 1200 TTCTGCTTTG AACTCCTGCT GCTTTGAGTC TCCCACTGCC AGCAAGCACT TCTCTGCCAG 1260 GCGGAGGGGC GGTGAAGGGA ATTAAAGGGG CAGTCAGTGG CTTGCCTCTG GCGGGAGGTG 1320 GCGGAGCGTC TCATTAGCGT TTGCTCCTTT CCTCCAGCTG GGCTTCACTG GGCCCCTCTT 1380 CTTATCAACC CGTCCTTCAC TTCACCCAGG CTGTCCCCTG CACTCAGACC CCCTCCAGTC 1440 CTTCCAACAA GATGGCAGCA GGATGACTGG GACTCATTGG AGCTAAGCAG AGAATTAAAG 1500 TTGCTTTTGT TCCAAACCTA AAACTTGAAA ATGAAGGAAC TCTTACGTGG AAATGCCACC 1560 ATCTCCCTTT TGTTTTATGC GTAAACCCAA CTGGTTCCCC ATCCTCTGGG 1610
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