Tag | Content |
---|
EnhancerAtlas ID | HS176-26248 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr3:57999400-58000620 | | Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_01957 | chr3:57997858-57999795 | Aorta | SE_01957 | chr3:57999811-58000554 | Aorta | SE_23194 | chr3:57999838-58000516 | Colon_Crypt_1 | SE_27681 | chr3:57993244-58000569 | Fetal_Intestine | SE_28779 | chr3:57993253-58000602 | Fetal_Intestine_Large | SE_30574 | chr3:57999545-58000564 | Fetal_Muscle | SE_37989 | chr3:57993219-58001698 | HUVEC | SE_41579 | chr3:57999804-58000450 | LNCaP | SE_45969 | chr3:57997854-58000623 | Osteoblasts | SE_52474 | chr3:57999733-58000569 | Small_Intestine | SE_65730 | chr3:57999912-58000986 | Pancreatic_islets | SE_69109 | chr3:57999816-58000591 | H9 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTAGATGGC CGTGGTGGTG CATGCCTGTA ATCCCAGCTA CGTGGGAGGC TGAGGCAGGA 60 CAATAGCTTG AATCCAAGGG CAGAGGCTGT GTTGAGCTGA GATCATGCCA TTGCACTCCA 120 GCTTGGGCAA CAGGAGCAAA ACTCCATCTC AAAAAAAAGT AGCAAAGTAG CATGCTTTGT 180 CAGAATTATT AATAACAAGT TGTGGGCCAT GTACAAGGTG GCACATTAGC ATTCAATGTC 240 ACTTGTGTAG TAGTTAAGAG CAAGGATTCT TGGTTCAAAT CCCACTTGCC ACTAAGTAGC 300 TATTAGAAAC TTCTGTGCCT TGGTTTCCTT ATCACTAAAA TGGGGATAAT AACTACCTTC 360 TTAAAAGGCT GTTATAAAGA TTAAACAAGT TAATAATTTT TAAAGTGCTT GGCACAGTTT 420 ATGGTACATA GTAAGTGCTC TGTGAATGCC TGTTAATTAA ATAAGGCACT GTTTAATAAT 480 CTCAAAAGTC ATGCCGGAAA GGTTTGCACA CTGAAAGGGC ATTTGAAATC AGCGCGCTCT 540 GGGGAGAACA GCTTGGTTGG CTAAGGTTGA TCCTACTTGC TAAAATACGG CTATGGACTG 600 CCTAGAGGGT GTCACCTCCT TGAAAGGGGC TGCCCCCTGC TATGTTATGG CTGCCTCCAG 660 GGCCCATTCA CACCAGCTTT GTTTCCAAGC TGGACAGGGA GCTCCAGGCG TCTGGTCATT 720 CCAGCCTCCC ACCCCTTTCA GGAATCTCTG GGCCAAATCA CTTCCAGATG GTGGTTGGGC 780 CTCTGTGGAG TTCTCCCAGC AACGGCGGAG CCAGCATGCC AGTCGGCAGC CGCCTTCGTT 840 CTTGGAGAGT CTGAGCTAAA GGAGGGCTTT GATTTGGAGC CAAATTGTGT CTCTTGGGTC 900 CTGGTTTTGT GCTGTGAGGC AGGTACCATG GAGTGGGCTG CTGGCTTAGT TGAGGATGGC 960 TGCCCTGCTC CTTAGGGGAG CAGATACCCA GGGCCTGGAG CCTTTAGGCC CTGCCTCCAG 1020 TAGCTCCATG GTCAGGGTGC CAGTCACCTT GCGTTTTCTT TTTCTTTTTT TTTGAGATGG 1080 AGTCTTGCTC TGTCGCCCAG GTTGGAGTGC AGTGGCGTGA TCTCGGCTCA CTGCAACCTC 1140 TGTCTCCCGG GGTCAAGCAA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGC 1200 GTGCGCCACT ATGTCTGGCT 1220
|
| |
|
|
|