Tag | Content |
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EnhancerAtlas ID | HS095-12043 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr17:2862430-2864720 |
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) |
MEF2A | MA0052.3 | chr17:2863253-2863265 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr17:2863253-2863265 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr17:2863251-2863266 | CTACTAAAAATAGAA | + | 6.57 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_31401 | chr17:2861487-2864472 | Gastric | SE_65245 | chr17:2859093-2864439 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 2862672 | 2863167 | chr17 | 2863440 | 2864256 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I002958 | chr17 | 2862229 | 2865246 |
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Enhancer Sequence | CCCACCCAGC CTTCTCTCCG GTTGCTCCTC AGATCCTCTC TTCCTTCTCC CCCAGCTGGA 60 GTCCCCTTCC CACAACTTTG CCCCACACAG GGTCTCTCTG AGCACAGCAT TCAGCCCCAG 120 TTAACCAGCC TCAGAGTGTT GTGTTGTGTA GAGGCTGCAG GGCTTGTCTG TTCATGTAGA 180 TCGGGTGCTT TCTAGGGTAG GGGTCTTGTT TTATTCTCCC TCTGTCTGTG CAATGGCTGA 240 TCCCCCTGGG TAGCGTGCCT GTTCCCTTTC AGTTGAGACT GTTGAAGCCA AATTTCTGGG 300 TGTTTAAGTC CCTACCATGT GCCCCCTGGG CCCAGCCTCA GAGGGTTCAC TCTTAGTAAG 360 AAGCTCACGT ATGGGGCACT GCTGGCCATG GAGTGCCCGC GTGGGCCTTG AGCCTGGGCT 420 CCATCTCTCT TCATCTTGCA CGTGTGGAAA CTGAAGCTCA GAGCAGTGAA GCGCCCGGGT 480 CACTTAGCTA GTTGTGAAGA GCTGAAACTG GAATCCGGGA TTCCCGATAC CTAGCCCAAG 540 AGTCTGGGAA CTGGGAGAAG GCAGAAGCTT TGGATTCCTT CAGTCCTGGG TTCAGGTTCT 600 AACCCTGACG CTTTCTAGCT GAGTATCTTC AGTCAAGTCG GTTTCCCCTT CTGAGCCTTA 660 ATTTCTTCAC TGAGGGGAGA AGGGGAAATA AAGATAATAC CCATTGTGGC CAGTTGCGGT 720 GTCTCACACC TGTCATCCCA GCACTTGGGA GGTCGAGGCA GGTGGATCGC CTGAGGTCAG 780 GAGTTCGAGA CCAGCCTGGC CAACCTGGTG AAACCCTGTC TCTACTAAAA ATAGAAAAAT 840 TAGCTGGGTG TGGTGGCACA CGCCTGTAAT CCCAGCTACT TGGGAGGCTG AGGCAGGGGA 900 ATCTCTTGAA CCCGGGAGGT GGAGGCTGCA GTGAGCCGAG ATTGCGCCAC TGCATTCAGC 960 CTGGATGGCA GAGCAAGACT CCATCTCAAA AAAAAAAAAA AAAAACAACA AAAAAAGACA 1020 ATACCTCTAG CAAAATAGCA CATGGAGGAG AGAGGGCCCC GTGCTGGGCA GTGGCTCTGC 1080 GGTAGGTTAT TAGGGGAGGG AGTGGCGTGG GGAGGGGATG GGAGGAAGTT TGCTCTCCTG 1140 CCCTCGGGGC TGTTCCCAGA CAGGGATGAC TAATGCAGGC CAAACAAAAC AGACTCCTGC 1200 CCTCACTGCC CCCACCCGCC ATCTGCCCAG TTTGCCAGCT GGGACAGGGT CTGTAGGGCC 1260 ACCCAGGTGG CTTTGTGTGT GTGTGAGGGG AGCGCCTGTT CAGTGGGAAC GGCCCTCCCA 1320 CGCCCTCCTG AACAATGCTG CAAGGCGACT CAGCCCAGGG AAGTCCGCAG AGGCTGCATG 1380 TCAATCCACC CAGTTAACAG GAGCCCTGCT GTCCACAGAG TGTGGGGTAC GTCACGCGCT 1440 TGGTGAGCCG GTGACCCGGC TTCAAATCTA GGCCCTGCCA CTCACTGGCT GTGTGACCTT 1500 AGGCAAGCAG CCTCCTTCTG GGGCCCCAGT GTCCTCGCTG GTGGAAAGTG CTGTGAGTTT 1560 CAAAGGAGGC CACAGAGAGA GCTAGCTTGG GAAGGTCAAA ATCCCTGTGC ATTAGTGTTG 1620 TGACCAGGCA GACGCTGCTT CTGGACTCCT TCTGCTTCAG AGGGGACCTG TTTCTTCTAG 1680 TTTGTGTACC GTCTCATACT GTCACCCGAT TTTCTCAGAT AGTCTTGGAA ACACCACGTG 1740 TTCCCCTCCT GCACAACACG GTTAAGTCAG AACTCAGTGA TAGAACTGCT GGACCAGGGC 1800 CAGGCGCAGT GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCTGAGGC GGGTGGATCA 1860 CCTGAGGTTG GGAGTTCAAG ACCAGCCTGG GCAACATGGT GAAACCCCAT CTCTACTAAA 1920 AATGCAAAAA ACTAGCTGGG CATGGTGGCA CATGCCTGTA ATCCCAGTTA CTTGGGAGGC 1980 TGAGGCAGGA GAATCACTTG AACGCGGGAG GTGGAGGTTG CAGTGAACCG AGATCCCACC 2040 ACTGCACTCC AGCCTGGGCA ACAAGAATGA AACTCCATCT CAAAAAAAAA AGAAGAGGCT 2100 GGGTGCAGTG GCTCACGCCT ATAATCCCAG CACTTTGGGA AGCCAAGGCG GGTGGATCAC 2160 CTGAGGTCAG GAGTTCGAGA CCAGCCTGGC CAACATGGTG AAACCTCGTC TCTACTAAAA 2220 ATACAAACAT TAGCTGGGCG TGGTGGTACA TGCCTGTAAT CTCAGCTACT CGGGAGGCCG 2280 AGGCAGGAGA 2290
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