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EnhancerAtlas ID | HS045-44832 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr3:57999660-58000560 | | 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 | CAAGGATTCT TGGTTCAAAT CCCACTTGCC ACTAAGTAGC TATTAGAAAC TTCTGTGCCT 60 TGGTTTCCTT ATCACTAAAA TGGGGATAAT AACTACCTTC TTAAAAGGCT GTTATAAAGA 120 TTAAACAAGT TAATAATTTT TAAAGTGCTT GGCACAGTTT ATGGTACATA GTAAGTGCTC 180 TGTGAATGCC TGTTAATTAA ATAAGGCACT GTTTAATAAT CTCAAAAGTC ATGCCGGAAA 240 GGTTTGCACA CTGAAAGGGC ATTTGAAATC AGCGCGCTCT GGGGAGAACA GCTTGGTTGG 300 CTAAGGTTGA TCCTACTTGC TAAAATACGG CTATGGACTG CCTAGAGGGT GTCACCTCCT 360 TGAAAGGGGC TGCCCCCTGC TATGTTATGG CTGCCTCCAG GGCCCATTCA CACCAGCTTT 420 GTTTCCAAGC TGGACAGGGA GCTCCAGGCG TCTGGTCATT CCAGCCTCCC ACCCCTTTCA 480 GGAATCTCTG GGCCAAATCA CTTCCAGATG GTGGTTGGGC CTCTGTGGAG TTCTCCCAGC 540 AACGGCGGAG CCAGCATGCC AGTCGGCAGC CGCCTTCGTT CTTGGAGAGT CTGAGCTAAA 600 GGAGGGCTTT GATTTGGAGC CAAATTGTGT CTCTTGGGTC CTGGTTTTGT GCTGTGAGGC 660 AGGTACCATG GAGTGGGCTG CTGGCTTAGT TGAGGATGGC TGCCCTGCTC CTTAGGGGAG 720 CAGATACCCA GGGCCTGGAG CCTTTAGGCC CTGCCTCCAG TAGCTCCATG GTCAGGGTGC 780 CAGTCACCTT GCGTTTTCTT TTTCTTTTTT TTTGAGATGG AGTCTTGCTC TGTCGCCCAG 840 GTTGGAGTGC AGTGGCGTGA TCTCGGCTCA CTGCAACCTC TGTCTCCCGG GGTCAAGCAA 900
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