Tag | Content |
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EnhancerAtlas ID | HS052-27021 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr3:127996360-127999050 |
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) |
RUNX1 | MA0002.2 | chr3:127998593-127998604 | TTCTGTGGTTT | + | 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 |
GH03I128277 | chr3 | 127996830 | 128000288 |
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Enhancer Sequence | ATGAGGGTGA TTGATTCACA GAGTGAGCCA GCCAGAGCTG TCTGTGAGTG ACAGCTGTGG 60 CTCCCCTGCC CTCCTGGGGC AGCATAGCTA CCTTAGCTTG CTGTCAGCTG TGGTGTTTGT 120 GAAGCTATCC ATTGTGGATG TGTAGATTAG GGTGAATCCC GATTTGTGTG CTCGCATTTG 180 CCTACCTGCT GGACTTACTG CCTGGCAGAC AGCTCTGCAC GTGAGCACAT GTGCACATAT 240 GGCCTGAGAT GGGGCCTTCC CAGGACAGGG GAGAGTTCTC TGAGGGCAGA TAGCAAGGGA 300 ACCAACCTGG GCTGAAGTCA GGGGAGGCTT CTCAGGTCCG AAGGAGGAGG AAGACTTACT 360 AGGAGAAGAT GAGCAAGGTG TGGGTAGAGA GGATTCTGGG CAAATGCAAA GGCCCCATGG 420 TGGGAGAGAG CCTAATGTGT TTGAAAACCT AAAAGGAAGG CATTTGGCAT CTGGACTGGA 480 GCCCAGAGAC AAATGTGGGG TGAGAGGTGC TGTAGAGGTA AGTGGCACCA GACCATGCAA 540 GGCCAGTTCA AGTTCTGTCT ATTCTTATGA CGCAGCTGGT TTTGCAGGGT GGGTGATGTA 600 GTGTGTGTGC AATTTATTTG TGTGTTTGAG GGAAAGACAG ATGGTTTGGA GAACAGATTT 660 GAGGGGAGCC AGGACCTTTC TGGGGACTAG TGGGGAGGCT GTTGCCATAG TCCAGGCAGA 720 TTGAGGTGGC TTGGATCAAG CTGGCAGCAA TCCAATGGGC ATTAAAGGCA TTCAGGAGAT 780 GGAATTAACA AGGCTTTGTG ATGGACTAGA TATAGGGACA GTGAAGGGGA GAGGCATATT 840 ACCGATGGAC CCCAGATCTC TGGCTTCAGT GACAGGCCAG GTGGAGGAGC CGTTGGTGAG 900 AGAGAATCCA GAACAATCTG GAGGGGAGAG TGAACAGAGC CAGGAGTATG GCTTGGGCTT 960 CACTAAGTTG GGGACGTTTG GGGAACCCAC TTGGAAAGGT CTAGGAAGCA AGCTGACATA 1020 AGTGTCTGAA GCTCAGAGAA GTTTGGGATA GGACATATAT TTATGTGCTG TTGGTGGCTC 1080 CAACCTTGGT AGTTGGGGCC TCTGGCTAGA AAAGAAAAGT TAAAAAGCAA GCTTCAGCTG 1140 TTTCATCTAA AGTTATAATT CCGATGCTTT AAAGGCTCCC AACCCTCTTC TTGTTCATGG 1200 TGGGGGAGCC TTCCTAGTTG TGAAAGGGTC TGAGTGGCTC CAGCTTTGGC ATATTAGGGT 1260 GCAGGGGAGG GTATTTCTAG GGACACTCTG GGAGAAGCTG CCCAGCCTGC ATGGTGCTAG 1320 TGCCAGTCTG CAAAATCTCC AGGTAATAGA GAGGGCAGGC CCCTGCCCAC CCCCTTGCAG 1380 CCTCCAATGC TGCTGCTGTG GCAGCTGCTG CTGCGAAACA AACCAGGGTG ACTGGGCGGA 1440 AGGTCAGGAG TTTAAGAGCT TGTTTGATTC AAAACTAGGC TAAAAGACAG GAGGGGAGTG 1500 AGCTGGTTTT CTGTGTGGAT CCTGGTATTT TCCTTTGAGT TGGGGAGGAG AATGGTGGGG 1560 CAGGGAGGGA AGGCCGGCCG CCAGAGGGAA CGCTGCCAAG CAGAGCGCAG CTAATGTGAA 1620 CCATACGGCG GCGGCGTTGG GCAGTGGCGG CCATCTCCCG CCCAGCTTAG TACAGCCCTT 1680 ACTGCGGGCA GGGGTGCAGA CAGGCAGGAA GGCAGCTCGG GCTGTGCGGC CACTTAACCC 1740 TTCCAGTGCT GAACTACAAG CAGGGCTCCT TCACCTCAGC ACATTGATGT TTCAGCCAAT 1800 AATCCTCTGT CCTGGGCACT GTAGATGTCT AGCAGCATCC CTGGCCTCTA CCCACTAGAT 1860 GCCAATAGCA CCCTCTCCCA GCTGTGATGA CCACAAGTGT CTGCAGACAT TCTAAATGCC 1920 TCCTGGGGGG AAATTATCCC TGGCGGAGAA CCAGTGGCCT AGAACAGGCG GCCCCCTCAG 1980 CTGCTGGGCC TGCCTGGACT CTGATGGGCC TGCACCCTTC AGGGGCCCTG CCCCAGACAC 2040 ACCACATCCA TGTTTGGAGT GCTGCCTGGG GCTGAGCATG TGGGGGTCGT TTTCCCATGA 2100 AGCAGGCAGC CATAGGGTCA GAGGGGAGAC GAGACCTACC CAGAGTTGTA TGCCAGTAGG 2160 AGCCAGGGTC CAGGATTGGT GTTGCTCCAC ACATTCCCTG TCCCCCTGCT CCCAGGCATG 2220 GCCCCCATTC AGTTTCTGTG GTTTTAAGTG GGAGGTGTGC AGCCTGCCCC TGACTGGCTT 2280 CCTGGGGGGA CTAATTCCTA TGCCAGCCTT CTCTGCCTAT TCAACATGCA GTTGCCCAAG 2340 GGAACATGGC ACGGGTGTTT ACCACACTGT TCTTATACCA AGAGTCAGTG CACACGAGCT 2400 CAGTGTCCAG CGGTGGGTCT GGTTCTCTAA ACCGTGCGAT ACCACGTGCC CATCGAACAC 2460 GATGGTGCAG ATCTATGTGG AAAGACCACC ATTAGAATCA TCAGATCCGC GAGGACAGAG 2520 ACTTTTGTCA GTCATGTTCC TGGGCCCTTA ATAAATGTCC TGTGAATAAA TAAAATGCTA 2580 ATTGCAAAAC CAAATCTCAA TATGTATGAT TTGGTCCCAT TATGTAGGAA AACTGTCTGC 2640 ATATGTTTGT ATACAAATGC ATCAAAAAAT CTGGAAGGAG ACAGCAAACT 2690
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