Tag | Content |
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EnhancerAtlas ID | HS040-00615 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:16504880-16505930 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16504928-16505810 | Colon_Crypt_1 | SE_23751 | chr1:16505381-16505879 | Colon_Crypt_2 | SE_26540 | chr1:16504790-16512175 | Esophagus | SE_28102 | chr1:16504631-16506039 | Fetal_Intestine | SE_29455 | chr1:16497964-16506131 | Fetal_Intestine_Large | SE_31527 | chr1:16504910-16506069 | Gastric | SE_34268 | chr1:16504832-16506037 | HCT-116 | SE_34628 | chr1:16497415-16506115 | HeLa | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16505086-16505424 | Pancreas | SE_50427 | chr1:16504889-16506043 | Sigmoid_Colon | SE_52536 | chr1:16504905-16505949 | Small_Intestine | SE_56795 | chr1:16504922-16506165 | VACO_400 | SE_57939 | chr1:16505036-16505756 | VACO_9m | SE_65472 | chr1:16505102-16505913 | 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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| Number: 1 | ID | Chromosome | Start | End |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | AGAGACGGGG TTACACCATG TTGGCCAGTC TGGTCTCGAA CTCCTGACCT CAAGTGATCC 60 ACCTGCCTCA GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCACA CCTGGCCTTC 120 TTTTTACCCT TTTCATTTTT TTTTCTCTTT TCCTTTTAGA AAGCAGGTTG TTAAACATTT 180 ACCAGCTCAC CACTGGCTGG AGGCCACAGC ATTTATAGCG TCTCAGAAGG GTCTGGAGCT 240 TAGAAAGTTT AAGAGCTTAG CAAGACTCCT CCTGTGTCTC AGGACCTGTG ATGGATCTGA 300 GCCTGTCTGA CACCAAAGCC AAAGAAATGC CTTCCTTCCC TCACGAGGCC AAGAGTTAGC 360 GTCTCTTTCT ACCCCATCAT GACAACTTCC TGTCCAGGGC AAGAAACTGT CCTGATTGTC 420 CCTTGGGGGC AGGGATTAAA GGTACTACAG GTTCAGAGCC CCTGGCTAGC GTGCCCTGCC 480 CTCTGACCAC GTATGATCAA TTCCATAAAT ATTTACCCAG CGCCTCACTT AACCTCCCTG 540 AGCCTGTTTC TTCAAAGCTG CAAAATGGGG CCCTTCAGCC TGACTACTTT AATTCATCCA 600 TCCACCCATT CCTTCAGTTA GCGGCTCCCC TGTGCTGGGT GGTGTTTTTG AAGGATACTG 660 GAGTCGGGAT GCCTGCTTTG AGTCCTGGCT CTGGCACTGG CTTCCTCGGT ACCATGGGCC 720 TCAGCGTTCC CATCTGTACA ATGGCACCCA CATAAGGGTT CCTTCCAACT CCTTTCCCCA 780 TCTCAGGGGG TTGTTGCGGG ATATCGGGGC TGGGGAACCT TGGCTAGCTG AGGAACTAGG 840 CTAGCTGACA CACAAAGGAC CAGCAACAGT TCACGCCCTG GAGACAGAAC GCGCCCACGT 900 GATTCACACC GGCAGCAGCG GACTCTGTTT CTGTTGCCTT GAATGAGGTG CGCTCTAGTC 960 TTGCAGAGTT TAGAAAACAA GGAGGTGTGG AATGTTCAGG GAAGACTTCC TGATGAGGTA 1020 ATAATAACAC AGGAACAGCT AATATTTGAT 1050
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