Tag | Content |
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EnhancerAtlas ID | HS050-25064 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr16:11705740-11706950 |
| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_10082 | chr16:11705586-11708566 | CD14 | SE_23656 | chr16:11705744-11708148 | Colon_Crypt_1 | SE_27070 | chr16:11705764-11708228 | Esophagus | SE_31920 | chr16:11705719-11708162 | Gastric | SE_42648 | chr16:11705745-11708264 | Lung | SE_50207 | chr16:11705709-11708328 | Sigmoid_Colon | SE_52871 | chr16:11705643-11708238 | Small_Intestine | SE_53430 | chr16:11705562-11708227 | Spleen | SE_61608 | chr16:11668804-11735966 | Toledo |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 11705983 | 11706695 | chr16 | 11705813 | 11706791 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I011611 | chr16 | 11705658 | 11710497 |
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Enhancer Sequence | AAACTCCTGA CCTCAGGTGA TTCGCCCACC TCGGCCTCCC AAAGTGCTGG GATGACAGGT 60 GTGAGCCGCT GCGCCTGGCC CTCCCATTTC GACTGTTGTG GGGTCCCACA GGATATGGAG 120 TGTGACAACA ACCCCCATCC AACGCAACTT AATGGCTTCC TTCTTCCTTC TTCCCCTCGG 180 GGCTCGGAAA TCACCACTCG CCTGGCAAAG AGGGTTATGT GGGTGCCCAC ACAGCCATGT 240 CACTGAGAGG GTGGAAACAG GGTCTCAAAG TCCAAGGATC TCCTGGCACT GCCCACACCG 300 CCAAAGCTCA GGACAGCCAA CCATGTGCCA GGTTTGCTCA GCCCAGATCT AAAACGGGGG 360 TCTCTCCAGT GAGTCAGACC AGGTCATTTC CCAGCCCAGG GACTCTGTGA CTCCTGGGAG 420 CCGCAGCAGG CTTTGGCTGC ACCGTCCTCA TCATTCTTGT GAAAAGGGGC CACCTGGGGG 480 GCAGCCTGGA GGGTTGGTGA AGAGGTGTCT CCCTCCCTGG CTTGGCCTGG GCTCTCTGGA 540 AGGCAGGTGA AGAATGAGGA AGGAAGGGCC TTATTGGGCA ACTCCCAGCA GGTTTCTGTG 600 GGAACGGCTG TCTGACCTCG TGTGGGTCAC CTGCGGTTAG AGCAAACTGC ACTGCATGCG 660 GCCAGCGGGC GGCCAGGGCC GGCCCAGCTC AGGACGCTCA CGTGCACAGA GAACCTGGAT 720 GGAAAGTTAA CAAGGCCCAG GCAGGAGCCC TCGCAGAGAC AGCAGACCTT CCCACCCCAC 780 TCCCAGCCCA GAACTGGCCA CCCACTTCCC CACCCCATTC TCCCCTGACA TCTCTGTTTG 840 TCCACGTCCT TGAGAAGGGC GGAGGGACGA GGACAGACTG AAAAGAGATG TTTGGAGGAT 900 GAGTCCGCCC TCTTGGGGAA TGATTTCACT GTGGAACCAA GCTTGGTTAC ACCAGAAGCT 960 CTTGGGCACC ATCTCAGGGA CTCCCATGGC TCCTGAAGAC TTGTGGGAAC CCTGTGTCCC 1020 CCTAGAATCT TGACCTCCCA ACCCTGCAAA AGCTGTCATC TTGGGGCACA GCCGATGGCC 1080 TGGGTGCCTC TTGATGGGCA AGGCCAGCCA TTCAGGTGCT TCACTCTAGG TTTTTCTTTG 1140 GATTTTTTTT TATTTGTTTT TTGGGGTTTG TTTTAGATGG AGTTTCGCTC TGTTGCCCAG 1200 GCTGGAGTGC 1210
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