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EnhancerAtlas ID | HS007-11286 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr3:57999350-58000590 | | 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 | AGACCAGCCT GACCAACATG GAGAAACCCC ATCTCTACTA AAAATACAAA ATTAGATGGC 60 CGTGGTGGTG CATGCCTGTA ATCCCAGCTA CGTGGGAGGC TGAGGCAGGA CAATAGCTTG 120 AATCCAAGGG CAGAGGCTGT GTTGAGCTGA GATCATGCCA TTGCACTCCA GCTTGGGCAA 180 CAGGAGCAAA ACTCCATCTC AAAAAAAAGT AGCAAAGTAG CATGCTTTGT CAGAATTATT 240 AATAACAAGT TGTGGGCCAT GTACAAGGTG GCACATTAGC ATTCAATGTC ACTTGTGTAG 300 TAGTTAAGAG CAAGGATTCT TGGTTCAAAT CCCACTTGCC ACTAAGTAGC TATTAGAAAC 360 TTCTGTGCCT TGGTTTCCTT ATCACTAAAA TGGGGATAAT AACTACCTTC TTAAAAGGCT 420 GTTATAAAGA TTAAACAAGT TAATAATTTT TAAAGTGCTT GGCACAGTTT ATGGTACATA 480 GTAAGTGCTC TGTGAATGCC TGTTAATTAA ATAAGGCACT GTTTAATAAT CTCAAAAGTC 540 ATGCCGGAAA GGTTTGCACA CTGAAAGGGC ATTTGAAATC AGCGCGCTCT GGGGAGAACA 600 GCTTGGTTGG CTAAGGTTGA TCCTACTTGC TAAAATACGG CTATGGACTG CCTAGAGGGT 660 GTCACCTCCT TGAAAGGGGC TGCCCCCTGC TATGTTATGG CTGCCTCCAG GGCCCATTCA 720 CACCAGCTTT GTTTCCAAGC TGGACAGGGA GCTCCAGGCG TCTGGTCATT CCAGCCTCCC 780 ACCCCTTTCA GGAATCTCTG GGCCAAATCA CTTCCAGATG GTGGTTGGGC CTCTGTGGAG 840 TTCTCCCAGC AACGGCGGAG CCAGCATGCC AGTCGGCAGC CGCCTTCGTT CTTGGAGAGT 900 CTGAGCTAAA GGAGGGCTTT GATTTGGAGC CAAATTGTGT CTCTTGGGTC CTGGTTTTGT 960 GCTGTGAGGC AGGTACCATG GAGTGGGCTG CTGGCTTAGT TGAGGATGGC TGCCCTGCTC 1020 CTTAGGGGAG CAGATACCCA GGGCCTGGAG CCTTTAGGCC CTGCCTCCAG TAGCTCCATG 1080 GTCAGGGTGC CAGTCACCTT GCGTTTTCTT TTTCTTTTTT TTTGAGATGG AGTCTTGCTC 1140 TGTCGCCCAG GTTGGAGTGC AGTGGCGTGA TCTCGGCTCA CTGCAACCTC TGTCTCCCGG 1200 GGTCAAGCAA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG 1240
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