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EnhancerAtlas ID | HS184-20999 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr3:134069430-134070390 | | Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_00031 | chr3:134065074-134095135 | Adipose_Nuclei | SE_01585 | chr3:134068825-134070641 | Aorta | SE_05913 | chr3:134069050-134070794 | Brain_Hippocampus_Middle | SE_26603 | chr3:134066865-134074765 | Esophagus | SE_28406 | chr3:134069327-134071891 | Fetal_Intestine | SE_29244 | chr3:134069064-134073751 | Fetal_Intestine_Large | SE_31582 | chr3:134068984-134070634 | Gastric | SE_33911 | chr3:134068760-134073650 | HCC1954 | SE_42135 | chr3:134068975-134070670 | Lung | SE_43455 | chr3:134066770-134074827 | MCF-7 | SE_47606 | chr3:134069158-134070330 | Pancreas | SE_48676 | chr3:134068980-134070764 | Right_Atrium | SE_53035 | chr3:134069134-134070629 | Small_Intestine | SE_57611 | chr3:134069047-134069885 | VACO_503 | SE_57611 | chr3:134070034-134070589 | VACO_503 | SE_68802 | chr3:134069234-134070227 | H9 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAACTTGGGA ACAGAAGGGG CAGGGACTGG GAGACAAATG CTGCCATTCC CCAGAAGGCA 60 TCACCAACCT CTCCCCCTCC CTTTATTGTG GTGCTCTGGC TTCCAGGGAG GAAGGGGTGG 120 GAGGTTGGCA CCTAGGGATG GCATGGAGGC TCTGGGGAAG CCTTTCCCTG GACCTTGCCT 180 GGCTCAGATC TTTGTGGCCT TGATCAACAA CCCCTGTGAG TTGTTCTTGG GACCCAAACA 240 CTACAAGGCA TGGCTGGGAA CTGCTGCCCT GATAACAAGT GTTTCACCCC ACCCTTCCCT 300 TGCTGCTGCC CCTGCCCCTA TCCTCTCCCA GAGGGAGCCC AGGGCTGTCA GGGCCAGGCA 360 GGAGAAGCTC CAGGCAGGTG CGGCTCTCCT AGGGGTGGAG AGAGTTCTGA TTCCGCCTGC 420 TGTTCCCATG GCTGGGGCTG GCTACTGCCC ATGTGGCAGT CAGCGCCTGG GCCTGACTCA 480 GGGACCAGCC ATCTGGCAGG GCCAGTTCTG GGCTCACACA CCTACCTCCA CCTCCACCTG 540 CTCATTCACT CTGCTCCCCA AGCCCTCGGG CTCAGCTTCT CCTTCTCTGA CCTGAAGACT 600 CCACCCACAG AGTCCCTTTT ATCCTCTCCC ACCTCTCCCA CTTTCAGTGA ATGGCAATGG 660 GGGATGGGCA CCTGGCCAAG GAGGAAGGGC TTGGGAACTT TGGTCAGAAT ATCCTACAGG 720 GCTACTGATC AAGCAGGGCC ACCTGTGACA CCAGCGCAAG GACAAGAGTA AACACCTGTA 780 TAATTAAAAA GCTCGGTTAC GTCTTTTTAC CTGTGGCTCC TTCTGACCCA AGAAGAGCTA 840 CAGACTAATG TCTGCTAGCA AGAGTTCCTT CATTCTGCAC ATCCCAGCTG TCCTCCCCAT 900 CATGGTCCTG TGGGAGCAGA AAGGAAGCTG GAGAGGGGAG GCTGCCAGGA GGAAGCGATG 960
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