Tag | Content |
---|
EnhancerAtlas ID | HS187-17214 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr3:57997940-57999330 | | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_01957 | chr3:57997858-57999795 | Aorta | SE_27681 | chr3:57993244-58000569 | Fetal_Intestine | SE_28779 | chr3:57993253-58000602 | Fetal_Intestine_Large | SE_34631 | chr3:57990088-57998757 | HeLa | SE_37989 | chr3:57993219-58001698 | HUVEC | SE_41579 | chr3:57997963-57998549 | LNCaP | SE_41579 | chr3:57998870-57999356 | LNCaP | SE_45969 | chr3:57997854-58000623 | Osteoblasts | SE_50199 | chr3:57997904-57999381 | Sigmoid_Colon | SE_52474 | chr3:57997997-57999387 | Small_Intestine |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAAAAAAAA AAAAAAAAGT CATGCCCGAA TGGTTTGCAC ACCGAAGGGA CGTTCAAAAT 60 TAGGGGAGAA CAGCCTGGTT GTTTGTTTCT GTTTGGTTGA TCATACTCTT GCCATGGTTA 120 GTATTATTAT CTTTATTTAA AGATGGGAAA CAGGAGTGAA GCCACTTGTG GAGGTGACCC 180 AGCTAGCTAG TAAATGGTGT CTGAAACCCA GGTCTGCCCA GCTGTTGAAT TGGAGCCTTA 240 ACTGACTTGC CTTCCAGTTT CAGAGATGAG TAAAATACAG CTTTTCTCTC CACATCAGAG 300 GGTCCCTGCA ACACTAGGTT TGCAAGTCTT AGGTGTTAGG GTGGTGGCTG GATACCCACA 360 CTCTGAACCT CTGACCTTGG ACAAAATAGG GATGTCAGGG CCTTCCATGA TTGGCAGGAT 420 GAATCCTCTG GGCTGTGATG AAGGTCTCAC AAGTTGAGAG TCAGCCGGGA ATTAAGTGGG 480 ATCAGTTTGC CTCTTGTGTT TTCCTCATTG TGTTTTGGTT GGTTGGTTGA GATTTCCTAC 540 TACCCAATGG ATGATGTTTT ATTCCATCGT CAGGGAAGGT ATCATTGAAT GAATACAGGG 600 TTTTGTATGC TTTGGATAAG ACCAGACAGT TGTGGAGTCA TTAGAATTGT GTACATGCCT 660 CCAGCTCTGA GATAGGTGGT GTTTCAACAG CTGCCAGAGG ACTCTGGCTT TTCTGCCTAG 720 AATTCACTGA AAGACAACCC TGGCTATTGA TTCACATTTG TGGTTCATTG TAAGGTAGGC 780 CCCTAGGCGC CATCCAAAAG TTGAAAATTT CCTTACGTTT CTTGTTATGT GATGGGCAGT 840 TCATAGTGAG GACTCAGTGT CTTTAATTCC AGCTGTTTGC CAGGAGTTGG CAGTTTTATT 900 TACTTGTTTT TCCAAAAACC TTTCTGACAT GGGGCAGTCC AGCCAGCTGG GAGGAAAAGG 960 GGTCTCTCAG CCCAAGAATG ATGATCAAGG CCTAGAAGTT TGGGTGGTGT GTTTTGTTTT 1020 GGGCCTTTAG AGAAAGGAAT TGTTTCCTTT TCAGAGGATG TGGTCTAACC CTAAAGTTTA 1080 CTTGACTGAC TTAAACCAGG CCAGCGCCAG AGCAGGCAGG GTGCGTGTTC CCAAGACTTC 1140 GGGTCACTAG GCAGCTTCCA GGGTGGTGGG TCACTGGTCC AGTCAGCTCC TTTTCCTTCC 1200 TCTCCCTTTT GTGCTACTAC TACCAAAATA ATTTCCAAAT AACCTTAAGT TCTGCTCTTT 1260 CTTGCATGTC TAGCAGATGC CAGCATGTCT TTTGGGTAGT ACAGAGAGTG CTTAAAAAGT 1320 AGCAAAGTTG GCCGGACGTG GTGGCTCATG CCTGTAATCC CAGCACCCTG GGAGGCCAAG 1380 GTGGGTGGAT 1390
|
| |
|
|
|