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EnhancerAtlas ID | HS180-00589 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr1:17907790-17908940 | | Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_01537 | chr1:17907755-17910530 | Aorta | SE_23081 | chr1:17907816-17910457 | Colon_Crypt_1 | SE_23747 | chr1:17907830-17908823 | Colon_Crypt_2 | SE_24767 | chr1:17907837-17909560 | Colon_Crypt_3 | SE_26139 | chr1:17906023-17909400 | Duodenum_Smooth_Muscle | SE_26573 | chr1:17907965-17909539 | Esophagus | SE_28131 | chr1:17905874-17909536 | Fetal_Intestine | SE_29073 | chr1:17905814-17909766 | Fetal_Intestine_Large | SE_31687 | chr1:17907755-17908906 | Gastric | SE_34117 | chr1:17906048-17909807 | HCC1954 | SE_47562 | chr1:17907792-17908882 | Pancreas | SE_50079 | chr1:17907831-17909680 | Sigmoid_Colon | SE_52601 | chr1:17907734-17908893 | Small_Intestine | SE_65277 | chr1:17905681-17911473 | Pancreatic_islets | SE_68684 | chr1:17907877-17909598 | H9 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCAAGACTG TCTCAAAAAA AAAAAAAAAA AAAAAAAGAA AAGAGAAAAA GAAAAATACA 60 TACTTATACT AACAAAATTA TTCGTCGTTT ATCTGAAATT CAAGTCTGTG TCCTGTATGT 120 TATTTGGCAA CCCTGGCACT GGGGCCTCAG ACACTGCAGG TGGAATCCAG GCCCCGCCTG 180 GGAGGAAATG GGCCCAGGGC TGTTTCACCC AGGCAGCAGC TTCCTGTCCT CTTGTATCAC 240 TATGAGAGAG GCAGAATTGC AGATGGTAAT GAGTGAGGGC TTTGTCCTCA GCCCCATCTG 300 AGTTTGAATC CTGACCCTGC CACTTAGACT GTGGGGCTGG TTAAGTGACA TGTTGTCTCT 360 GTGGCTTAGT TTCATCATCA GTAAACATGG GGACAATGAT ACCCTCTCCT GGGCTGTTGC 420 AAGGTTTAAA TATATGTCAG GCGTGGGCAT GGGGTAATCA ATTGCTCACT GACGGGAGTG 480 CTTATCATCG TGGGTGTCAG CAGGACAGAC AGCGTGTGCC ATGCCCTGCA CCCCTGGGAG 540 AGCCAAATGA TGCATCTCCT CCTCCCTGAG CCTCGGGGTT CTTCTTGGGC GGGGGGTGGG 600 GAGCAGCACA GCAGACCTGT CTTCCCTGTG GCAATGGGTG GCTTCCTAGG GTCCCTCGCC 660 TCCTGGACTC GCTTGTATTT TCTCACAAGG ACCGGGTCTG TCCAGGAACA TCAGAGGCAT 720 GAGTGACCAG CTCTGGCTGT GCCACCTTTG CAGGCTATTA GGAAGGGCTT CCTTCAGCTC 780 TCAGCTGTGC TGGGATGGGC CTCCTGAGTT TTCCTTCTGA TAAGGAGCAA TGCCTGATTG 840 CCGGGGGGAG GATAGAAGGC GGCCTTGGAG ACAAGCACAT CTCACCTCCC AATTCATGAC 900 TGGGATTTGG GTCCCAGCAT GCCTGGCCTT GCCCCATCCC GCCCCTGCTG CCATGGGCAC 960 CTGTTCCCTT TCCTCTCCCC ACCAAGAGGC CTGAACCTGA ACATGGGGAG TGAGAAAAAA 1020 AAATTTATGA CTAAGTCAAT TCTGTTCTGT TCAGCAAACA TTTGACAAAT ATTTGTTGTT 1080 CCAGCTCTTT CTAATATTGC TGGCTAGTAT CATCTGGGTG AACCCAGCTC TTTGCCATTT 1140 TCTCATTCTC 1150
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