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EnhancerAtlas ID | HS092-28392 | Organism | Homo sapiens | Tissue/cell | HFF | Coordinate | chr3:57999750-58000570 | | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
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 | AACTACCTTC TTAAAAGGCT GTTATAAAGA TTAAACAAGT TAATAATTTT TAAAGTGCTT 60 GGCACAGTTT ATGGTACATA GTAAGTGCTC TGTGAATGCC TGTTAATTAA ATAAGGCACT 120 GTTTAATAAT CTCAAAAGTC ATGCCGGAAA GGTTTGCACA CTGAAAGGGC ATTTGAAATC 180 AGCGCGCTCT GGGGAGAACA GCTTGGTTGG CTAAGGTTGA TCCTACTTGC TAAAATACGG 240 CTATGGACTG CCTAGAGGGT GTCACCTCCT TGAAAGGGGC TGCCCCCTGC TATGTTATGG 300 CTGCCTCCAG GGCCCATTCA CACCAGCTTT GTTTCCAAGC TGGACAGGGA GCTCCAGGCG 360 TCTGGTCATT CCAGCCTCCC ACCCCTTTCA GGAATCTCTG GGCCAAATCA CTTCCAGATG 420 GTGGTTGGGC CTCTGTGGAG TTCTCCCAGC AACGGCGGAG CCAGCATGCC AGTCGGCAGC 480 CGCCTTCGTT CTTGGAGAGT CTGAGCTAAA GGAGGGCTTT GATTTGGAGC CAAATTGTGT 540 CTCTTGGGTC CTGGTTTTGT GCTGTGAGGC AGGTACCATG GAGTGGGCTG CTGGCTTAGT 600 TGAGGATGGC TGCCCTGCTC CTTAGGGGAG CAGATACCCA GGGCCTGGAG CCTTTAGGCC 660 CTGCCTCCAG TAGCTCCATG GTCAGGGTGC CAGTCACCTT GCGTTTTCTT TTTCTTTTTT 720 TTTGAGATGG AGTCTTGCTC TGTCGCCCAG GTTGGAGTGC AGTGGCGTGA TCTCGGCTCA 780 CTGCAACCTC TGTCTCCCGG GGTCAAGCAA TTCTCCTGCC 820
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