Tag | Content |
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EnhancerAtlas ID | HS043-26573 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr21:42618780-42621270 |
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) |
GCM1 | MA0646.1 | chr21:42620740-42620751 | GCACCCGCATG | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr21 | 42619081 | 42619274 | chr21 | 42619377 | 42620262 | chr21 | 42620714 | 42620758 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I041246 | chr21 | 42618648 | 42625146 |
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Enhancer Sequence | CTCCGTCTTC TCAACTGAGG GGTGGTTGTG AGTTTTGGGT CAAATGCTTG GTGTTTAGTA 60 GATGCTTGGA GCTTCCATGA AACATGCAAC CACGGCGTTG CTGCTATTTG TTCAGATGCG 120 AGAGGAACAT GACTTTTGGC TGCCTGAGTG TTCTCATAGC ATCTGGGCCT TCCTTGTGAG 180 ATCGTCAGAA AGTGTTTCCT GCACAAAGCC TGTACTGCGG CCCTGGCGTG GGGCTGATTG 240 TCCCGCTACT CTGCTGTGAT GGCTGAATTC AAAGAGTGGC CGATAGGAGC ACGTATGGTG 300 GGTGCCTTGT TAACAGCTCA TAGCAGAAAC GTGACAAGCG GGAGAGGGCT TTGGGTTGTC 360 CTGAACTTCA AACACCTGTA ACTGCTGCGG GAAGAGCGGC ACGTGGATGA AACGGACACA 420 GAGGGGGAAT AGGCAGGAAA GGACGCGGGC TCTTTTCGAA GCAGCAGGTC TCAAGGCGGC 480 CAGCCACTGG CGCAGCTGCA GCTGAAGCCA CGGCAGAGTC TCCATCCTTC CCACTATCTG 540 CTGAATCAGA GAAAGTGGCA GGCAACATTT TTAGTGCCTT AAATTTAGAA CGCTTGCTCA 600 AAATCAGACC CTACTTAAAA TAAGGAGCGA TACCCTCATT TCTTAAATAG TAAAAATGCC 660 CTCAGCAGAA TTAACGGGAG TATCTTCCAA CTTCATATCC TGAATGGAAA AGTCTGTCCA 720 CCATCCCGAG GACGTGTTTG AAGCGCAGTG TGAAAATCCA GCACGTCGTG GACCGGCCAG 780 ACCCCTGTGC CGTGAGAGGC GGGGCGGCGG GGCCGTGGGG CGCTCGCACT CCCGAGCTCA 840 TCGTGGCATG CGCTGAGCCG AAAACCACGA GGTAGAGGGA ATGAGATCAC AACATTTGTT 900 TGCGTTGTCT AAAATTATCC TCTGATTTCA TTCGGTGCCT GCGTCAGGAG GGAGAAACAT 960 GGGAAGGTTG TTTGTCTTGG GCAGGGAAAG CATCACAAGG GCGCGTTGTG TGTCTGGCTT 1020 ACCGTCTCTG GACCAAAGCT GTGTTTGTTT TTCTTATCTA CCAGTTCCAG TAAGCCAAAC 1080 CTCTTGGCGT GGGTTTCCTT CTGGTTAAGG GGAGGGCTGG CTTCAGAGAG TGAAAGACAA 1140 TAAAAACGTG GAGCTCTGTC CCCTGGCATG GATTGTTCAG ATGGGATTCT AGAAATTAAG 1200 GGTTTGGAGT TCTGTATTTA GAAATGAACC TGGAGCGGGG AGTGTTGTAC AAGGTGCAGC 1260 CCATGCAGAG GCACCGAGAC CTGGGCTCGT TCCGACCCTG CCGCAGTGCC CGCTTGGCTC 1320 AGGCCCAGCG CCTCTCTACG GAGGAAATCC AGACGCAAAA TAATACCCGC TTGAAAATGG 1380 CTTCTAACTT TAACACTCTG TGATCTGAGG GTCGAAACTG GCTCCCAAGG ACACGTGGCT 1440 TCACCCCCAG GGAGGCTGCC AGACTTTTGG TTAAGGACCA TGGCTCTGGG GACAGTAAGT 1500 CCCACATCCG AATCTGAGGT GAGCTCCCCA GGCCAGTCAC TTGGCCCCTT GGAACCTCCT 1560 TGTCCACCTG CCGTTGGAGC TGGTCATGGC ACTATCATCT GAGCTCTGTA CCCCGTGTCC 1620 CGCTGCAGAC CTGGCCACCG AAACTCTTCC CCGAATCCAG CAAAATGACC ATCCCACCTC 1680 TTCTGAGCAT GTCTGAGAAG GGGCTCTCCC TGTGATGCAC ATCTTCAGTA GACTTCGCTT 1740 TTTCACAAAG CAAAGATGCA TTAATGCCAG CATTAGAAAT TTCACAAATC AATCACAAAT 1800 GGTCTGAGTG GAGAACATGG GATGGATGAA CCAACCACAG GGTGCTTTCT CCCCAGCTGC 1860 ACGCCCTGGT GAGGAGGGCA GGTGTCTGCA GTGCGCGTGG TTACGTGGCA CGTACCACCC 1920 CTGATATTCA GTGCGTGGAC ATCGGCAGAT GCATACAGGG GCACCCGCAT GTTTTTTCAG 1980 TTGTGGTCTT GGCAGCGTTC TGTCCCATTT TCCTGTCTTC TGTTCTAACT ATCCTTTTGG 2040 TTTCTATAAG ACTCTTCTCC CTCCTCCTTG GACTCTCCCT GTCCCTGTGC CCCTCCTCGT 2100 GGAGCCTCTT CTTCTGGCCT GAGCCACCTG TTCTTGCTGC ACACCCTCCT ACGTGATCCC 2160 ATCCTTAGCC TCATCGATAC CTCCTGCTCA CCTGTCAGTG CCTCTGGAGT GTGTGTCTAG 2220 CCCAGGCCCA TCCCCTGGAA CTCAGGGGAC TCAGGACTAG TGGGCATGTA CACTTGGCCT 2280 CAGGGGACTC AGGATTAGTG AGCCCCACAT GTACACTTGG CCTCAGTGGA CTCAGGACTA 2340 GTGAGCCCCA CATGTACACT TGGCCTCAGG GGACTCAGGA TTAGTGAGCC CCCACATGTA 2400 CACTTGGCCT CAGGGGACTC AGGATTAGTG AGCCCCACAT GTACACTTGG CCTCAGGGGA 2460 CTCAGGACTA GTGAGCCCCA CATGTACACT 2490
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