Tag | Content |
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EnhancerAtlas ID | HS058-03982 |
Organism | Homo sapiens |
Tissue/cell | GM10847 |
Coordinate | chr19:45622980-45624320 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_31565 | chr19:45622597-45623259 | Gastric | SE_31565 | chr19:45624096-45625697 | Gastric | SE_65319 | chr19:45615291-45623609 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 45623609 | 45623659 | chr19 | 45623666 | 45623849 | chr19 | 45624187 | 45624318 |
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Enhancer Sequence | CAGACCACTG GGAAAGTGGC CAGGTAGGGC TGTGTCTCTT GTGGCTCTGC ACACATGAGA 60 GGTGGTGGGT GTGGTGCTCA GAGAAGAGCC AGCTCCACCC CCCAGCACCC CGCACAACCT 120 TGCTGTTTGA AGGAGGCCGC CGCCCCAGGA GGGGCTTTAG GGGCTGCCAG GAAGCCCGGA 180 GAAGGGCCTG GGGTCCCTCT TTGTTCCTGG TTCCCGGCTG CTTCACTGGC TACTCCATCT 240 CTGTGTTCAT TTGCTTTTAA ATGAGGAGCA CAGATTTTTT ATTTTCCCCT TCTTTTTTTT 300 TTTTTTTTTT TTTGAGATGG AGTCTCACTC TGTCGCCCAG GCTGGAGTGC AGTGGCGCGA 360 TCTCCGCTCA CTGCAAGCTC CTCCTCCCAG GTTCACGCCA TTCTCCTGCC TCAGCCTCCC 420 AAGTAGCTGG GACTACAGGT GCCCGCCACC ACGCCTGACT AATGTTTTGT ATTTTTAGTA 480 GAGACAAGGT TTCACTGTGT TAGCCAGGAT GGTCTCGATC TCCTGACCTT GTGATCCGCC 540 CACCTTAGCC TCCCAAAGTG CTGGGATTAG AGGCGTGAGC CACCGCACCC GGCTTTCCCC 600 ACTTCTTGCA TAAAGGGTAG CATTCATGAG CATACCGTTC TGCACCTTGC TTTTTTCATT 660 TGTGTCTTGA AACCTGTTCC CTGTTGGCTA AGAGAGCGCA CACTCATTCT CTGTGGCGGC 720 AGGGCTCCAC TGCGTGGATG AACTCTGGGG AGCTAGCCGG TCCCTGCTGG TGGATATTGT 780 GGTTGGTTCC GGTTCTGCAT TCACAAGCTG CTGCAGTGAC TGTCCTTACA TGTATGATTT 840 TTCATCTTTG CAAGTATGTC TGTAGGATTA ATCTCCAGGT GTGTAATTGC TAATCAAAGG 900 GTATATGCAT GTTACTTTTT TTTGAGATGG AGTCTTGCTC TGTTGCCCAG GCTGGAGTGC 960 AGTGGCGCTG TCTCATTGCA ACATCCGCCT CCCAGGTTCA AGCGATTCTC CTCCCAAGTA 1020 GCTGGGATTA TAGGCACCCG CTACCACACC TGGCTAATTT TTGTATTTTT AGTAGAGACG 1080 GGGGTTTCAC CATGTTGGCC AGGCTGGTCT CCAACTCCTG ACCTCAGGTG ATCCACCTGC 1140 CTCAGCCTTG GCCTCTCAAA GTGTTGGGAT TACAGGCGTG ACCCACTGTG CCCCGCACAT 1200 TTGTACTTTT GACTGGTCTT GCCAAATTGC CTTTGAGACG GAACCATGTC CTTGGTCAGG 1260 TCCTTTCTCA TCTCTAAGCG TCCCCTGGAA AGTTGGGGAG ATAATTTCTA TTTCTCAGGG 1320 CCATTAGGAA GTGGAAACGA 1340
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