Tag | Content |
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EnhancerAtlas ID | HS134-24382 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr17:36103510-36104530 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23266 | chr17:36101321-36107651 | Colon_Crypt_1 | SE_24029 | chr17:36101860-36106566 | Colon_Crypt_2 | SE_25028 | chr17:36101208-36107357 | Colon_Crypt_3 | SE_29293 | chr17:36100241-36108294 | Fetal_Intestine_Large | SE_32396 | chr17:36101682-36107120 | Gastric | SE_47579 | chr17:36101881-36106462 | Pancreas | SE_65485 | chr17:36101485-36106876 | Pancreatic_islets |
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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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Enhancer Sequence | CCCACCCCAA ACCGCCGCTG CGGACGTGCG GCCAAGGCTC AGCCCCGAAA TCGCGGCGCT 60 TCAGTGTCCG AAGCCACGCG ATGGGCTCTG TCCTAAAGCG GAGTGGCCCG GGAGCGACGT 120 GCTGTCTCAG GGAACCGCTC GGCTCCTTAG ATAATTAGTA ACCAGCTGTC AAAGTCTAGG 180 GCGGTCGGGG AGGACCCACA AACGATCCCG GCCCTGGGGA TACACTGCCA GCCGGCCTGA 240 ACTCCCGGGG AGAGGCCGGG GGTGGGCAGC GAGGTCTGGA AACGCCCTCC TTTCTCAGAC 300 TGAGACCAGA TCCTCTGCGA ACTGAGGTCT GAGACGCGTT CGCCCCCACA CCACCGCGCT 360 TCGTTTCTTT GGCCCCGCGC GTGTCCACCC GGACCCTGCA TGGAACATGC CCTTTGCAAA 420 TCTAAACCCG CGTTGGGGAT CCCGGATAAT TCCGGGCCTT GCATGGGCGC GGCTAACAAG 480 AGTGCCCACC AGGGAACTCG CCTCCCAGAT CCCGGCTCCG GATGCCGCCT GTCCTTCGGC 540 AAAGAACTGC AGGTCATCAT GCAGGTCAAT GTGTCCGAGG CCGACATGCG GCTTTCCAGA 600 CCCGAGGCAG CGCGCAGGAA AAATGCGCGG CCTGGGGCTT GCAGCGGCGC GAGGCTCTGC 660 TCCCGGGAAG TCGCAGCGGT TTCACTGCAC CCACTCGCAC CTTCAGTCGC GTGGGCAAAC 720 CTCCCGGCAA AGGGCTCCAC AGCTCCAGTT CTCCCCGGCC CAGCCCCAGC CCCGCGGGGA 780 AAAGCCCTTG GGTCTCGGAC GCTGGCCTGG GCCTGGGGAG AAGAAGCCCG GTGGGCCGCA 840 GGGTCGTCCC GCTAAGGGAT TGGGAAGGGT CCGGGTGTTG GGAGAGAAGC AGAGCGCCCC 900 CCGGGGGACT TCTCTGGTGG GAAACGGGCT TGGCGAGTGT GGTCGGGCGC AGTGTCACTC 960 AGGCCCGGGG CCGGGGCTCC AGGGGTTCGG GTGGGTCCCC TCCACCTCGC TCTGCGCCTA 1020
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