Tag | Content |
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EnhancerAtlas ID | HS139-17382 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr14:92357680-92359580 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_01578 | chr14:92354979-92360399 | Aorta | SE_47626 | chr14:92358153-92358483 | Pancreas | SE_47626 | chr14:92358562-92359114 | Pancreas |
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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 |
GH14I091889 | chr14 | 92355377 | 92360470 |
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Enhancer Sequence | TCTGGAAACA GAAATGCAAG CAAAGTGAGA CAGGTCTCCT CACTCAATGA TGCCCCCACT 60 AGCATGGCAT GATTGCCTTG CTCTTCCCAA ACAGGATCAT GAACGGAAGC AAATGGGAAC 120 AGGAGCCAAG ACAGTGCCTA CTGAGTGTCA CGGATGGTGA TGCTGTCTCG AATACAAGGC 180 TCAATCTCCC CACAATCTTT CCCCTCCTCG ACCCATCTCA GTCCCATAAA TACCTGAACC 240 TATCCTAAAA GTTGCAGAAG AAATTTCTGC TTCGATTGGG ATGTTGGGCA AAATGAGCTC 300 TCCAATTTTA CCCAGCTCTA AGATTCAACA CTAAGGTTTA TCCAAGATGG ACTCTCCAAT 360 TTTTCCCAGC TCTAAGATTT GAGATTACCC AGCTCTTAAG ATTTATCCAA TGTTAAGATT 420 CAACTCAAAG ATTCCATATA GAGGCTCCAC TGCCCAGGAT TCTTCTTAAC ACGTAAGAAG 480 AATCCATAGC ATCACTCCAA TAGGCTCCTT GCCAGCTCCA TGAACAATGA ATATGTCCAG 540 CTGTCAGGAA CAAGAGCCAG TTAGGCTGGG ATGAGCTGGG CAGCATGACC CTGGAGACCC 600 ATGAATCCAG TAACATGAGG GCACTGGAAT TCACCCTGAA TCTCCTCCTT GCACCAGAGT 660 GAACATAAAA CTCTGGATAA ACACATCTCT TCCAAGCCAC AGCTGGCCTT GCCAGGGAAA 720 GCGGCGGCAC TGTGGGTGAA TGGATCCTTT GAGCAGAGCT GGGCAATGTG ACCTCCCTGT 780 AATATGTATC CATCAATGGG GAGCCTGATG TCATTGGGAA AGCACTTCTC AACACCCCAA 840 GCTGATGTGA TAATGGGCTG GAGAATTCAT TCCTGTGGGG TAAGGGTAGT GAATGAAATC 900 ACCGGCCTCC TGGCAGAGTC TGAGATGGCA CCAATACAGG CTCCTGCTGT GACCAGTTGA 960 TCTGACTGTA GCTGGAACTG GTCCTTATCC CCACCTCCCC CAATCTAACC AGGTTTCCTC 1020 CCTGGTCCCC CTGTTCCTTT GGAACCAGGG GCCATCCAGG ACTCTGGAAG CCGGCTTAGA 1080 GCCTCAGTCC TTGTGCCTGG TTTCTACCTA CTGCCAGGAA GGACTCCACC TCCCAGATCC 1140 ATCTTGATCC CTTACCTATT GTTCAGCCCT TCTCAGATTC TGTGCCCTGT CCTGTGATTC 1200 TGTTTTGTCT CTAAGTCCCG GCTACTTCTA ACCTGGCCAC TGCACTGCCC CTGAGTGCAG 1260 AGCAGCTCTT GCATAGAGGG CCCATTGGCT GTACAGTGGC TGGCCCTGAC TTCTTCCCAG 1320 AGTGCAGTTG GGCACATCAC CAAGGCCAGG CAGGCAGCAG GGGCTGGAGA GGGTACCCTT 1380 CACTACGGGT ACCTTGGAAA AAAGGCAGCC CCCCTGACCC CTCATTTTTC TGCAAAAGCA 1440 GCATCTTCAG TGGTACACAG AACAGACAGT GTGTGGCTAT GGAACTTGCA TTTTGAAAGG 1500 GAAAGGTGAG TTTAGCCAGG GGAGGGCAGG AGTTCAGCCA TAATTAGGCG ACGTCTTCCT 1560 TTCAGATGTG AATATGAGTG GCTGGGCCAC ATGGTACCAT GCTAGGCATC CATGAGCATC 1620 CTTTCCACAG CTCCATGCTC CCAGGAAGAG AACAACCCTC CCAGGTAGAG GAATGTCCGA 1680 GTTGCTGGCA CCCCTCACAT CAGAGGGTTT CTGTAACAGG GCTGGTATAG CCCGGTCTCC 1740 CCCTACCACT CCAGCGCCCC TTGTGGTGGG AAAAAAAAAC TAGACTGAGA CACGGGAGAC 1800 TTGGAAGTTA GACCCAACTC ACTTTGTCTA AAATGTTCTT TCTCTATGAG TCTCAGTCTG 1860 CGATGCTATA AAAGTTGGAT GACATAATAT TCAACATCCT 1900
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