Tag | Content |
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EnhancerAtlas ID | HS111-01515 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr14:102993470-102994610 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_23111 | chr14:102993576-102994723 | Colon_Crypt_1 | SE_23755 | chr14:102993584-102994578 | Colon_Crypt_2 | SE_24691 | chr14:102993552-102994712 | Colon_Crypt_3 | SE_26698 | chr14:102992193-102995757 | Esophagus | SE_31972 | chr14:102993558-102994751 | Gastric | SE_34746 | chr14:102990235-102999537 | HeLa | SE_43092 | chr14:102993596-102994641 | Lung | SE_50471 | chr14:102993595-102994696 | Sigmoid_Colon | SE_52460 | chr14:102993473-102994792 | Small_Intestine | SE_68019 | chr14:102974923-103027639 | TC32 | SE_68438 | chr14:102968025-103022180 | TC71 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 102993679 | 102994550 | chr14 | 102993844 | 102994139 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I102522 | chr14 | 102989325 | 102995336 |
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Enhancer Sequence | TCAGCTCACT ACAACCTCTG CCTCCCGAGT TCAAGCGATT CTCCTGCCTC AGCCTCCCAA 60 GTAGCTGGGA TTACAGGCCT GCACCACCAG ACCCAGCTAA TTTTGTATTT TTAGTAGAGA 120 CGGGGTTTCA CCATGTTGGC CAGGCTTGTC TTGAACTCCC GACCTCAAGT GATCTCCCTG 180 TTTTGGCCTC CCAAAGTGCT AGGATTACAG GCGTGAGCCA CCACACCCAG CCTCACGTGG 240 ATTTTTGATA AAGCAAGGTT CTTCTGTGAT AGCAGCAGGC CTCCATTATC CTGGTCAATT 300 GGCCTGCACA ACTAGGGAAA CAATGGTGGA AAACTTCGAG AAGCTTGTGT TCCACCTGCC 360 ACCAATGGAG AAAGCACCAC TCCACTGTGA CATGCTTCCT GATGACTCGC TGAACAGAAG 420 GATGCACCCT CAGCCACCAA GGGTGTAGTT TGTGGGTGCC TCCTGGGAAC ATCAGGTTGG 480 CAACACAAAT GCCAGCCCCT CACCCTAGAG TGATTTCAGA GTGTCTCATC TCTTAACTCT 540 GAGTCACAGA GCGGTGGGGA GGAAGACATG GGGCAGGGCA GGGCAGGGCA GGGCTGGGCG 600 TGGCGTGGCC ACTCATGGAG CAGAGGGAAG GGTGGAGAGG TGCACTCTGA GTTTGTTGCC 660 TTCATTTGCT TTGTTGATGA AGGAGGAGCC TGAGGGGCCT GGCAGTGGGA CTGAGGCTCT 720 GGGCCTTCCT GCTCCCCTGG GTTTGACCCA GACTCCAGCT ACCCAGGCAT TGCCAGGCAG 780 TATCCTGGGG AAAGGTGGGA CCTGCTGCTT CCCACGCCTG CCCTGTGGGA TGGGGAGGGC 840 TTGGGGAAGG TGCTGCTATG CCCTGAGTCC CCGGAGCCAA AGACTCCCGA GGGTGACAAG 900 CAGCCCTGCC CGACCTCAGG CCCAGGGGTG ATGGCTGTTG GTGGCTCCCA GGCTGAGTCA 960 CTGTAGCCTT CCCGTCACTC TCTCTGACAC CCAGAGACTG GGTCCTGCCA TCCTGGGGTA 1020 AGGCAGGGGG CAGGAAGGTG CTTTCGAGAA TGTAGCCCTG GCCGGGCACA GTGGCTCACG 1080 CCTGTAATCC CAGCACTTTG GGAGGCAGAG GTGGGCAGAT CACCTGAGGT CAGGAGTTTG 1140
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