Tag | Content |
---|
EnhancerAtlas ID | HS092-15691 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:35805560-35806560 |
Target genes | |
| Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_01165 | chr14:35804585-35807755 | Adrenal_Gland | SE_23298 | chr14:35805483-35807654 | Colon_Crypt_1 | SE_24327 | chr14:35805505-35807540 | Colon_Crypt_2 | SE_26613 | chr14:35804098-35807686 | Esophagus | SE_27693 | chr14:35800617-35807759 | Fetal_Intestine | SE_28626 | chr14:35800494-35807947 | Fetal_Intestine_Large | SE_32027 | chr14:35804417-35807628 | Gastric | SE_34130 | chr14:35804231-35807631 | HCC1954 | SE_34831 | chr14:35800577-35808006 | HeLa | SE_41762 | chr14:35805560-35807508 | LNCaP | SE_42211 | chr14:35804395-35807731 | Lung | SE_47013 | chr14:35805519-35807575 | Ovary | SE_49399 | chr14:35805440-35807651 | Right_Atrium | SE_50091 | chr14:35804226-35807720 | Sigmoid_Colon | SE_52425 | chr14:35800645-35807722 | Small_Intestine | SE_53368 | chr14:35804110-35812246 | Spleen |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH14I035330 | chr14 | 35799980 | 35812312 |
|
Enhancer Sequence | CTACCTGACC CATAGTTCTT AAATTTAAAA TCTTGATATG CTGGTGGATA TGCAGCTTGA 60 TTTCTTTAAG CCGACATGGC CTGACTTTTT CAGATTCTCA GCCTGTGTTG GAGGGCTGTT 120 GAGTGTTCTT TCTATGCAGA AAGTACGCCT GCCGTCCTCT GTTTTGTAAT CGCCACCCCA 180 TCCCTGCCCA ACACACACAC CCACACAGCC GCAGTTACGC CGGGTCCAGC AACGCACGAA 240 CCAAGTGGAA GGTCAAGGGC TGGGGCTCCG TTTCCCTCCC CTTGAAGCTG TTTGGTTTGC 300 TCTTGTCCCA GCCCCTGACT GAGCCGCCAG CCCAGAACGG GGGCAGCCCT CCCCCATGCA 360 GTCAGGGCCA GAGGAGCATA ATATTGCCCC CCCGGGTGCA GCCTTAGGTG CAGGAGCGTT 420 GGGAATTTTC CATCTTGCTC TGCAGCCTGG CTTCTTAGGT CATCGTCCTG CTGCTGACAT 480 AGGCCTGGGT TGGGCGAGTT TCCTGCAGGT CAGCGAGGGC GCGGAGGCAG CGCCTGAGCC 540 TGCTCAGGGC CTGGCTTCCT GCCTGCTGTG AGGAAGGGTG GAGGAGGGGT TCGAGGCCTC 600 AACCATCCCT TGGCCCAGAG CCTCAGGCCA AGCAGCCTCC GCCTCTGCCC AGGCCTGTCT 660 CCTCCCGGCC TCCTGCTCTC CTGTTTCCTA AAGCTTTCCC GCTGGGTGGC TCCCAGTTCT 720 TCCAGAAATC CCCTCCAGGA AATTTGCTTG TTGCCACAAA ATAATGCAAA TCTGTTCCTG 780 GGGCCGCCCA GGCAACCTGC AGTCTCTGTC TCCCCAAGAC CTGAGGAGGG AGGGCGAGGC 840 AGGCCCTGTG CCCGTCAGGG TCCCTTTTCC AGCCATGAGG ACAAAGGATA AGCCGCACCC 900 TCGTCACCCT CTCATAAGCT GCAAGAGAAA GTTCCTGGTT TTACCTCTAA GGGAACCAGC 960 TCCACCTAGG GAAAGGCCAC ACAGGACCCT CAAAGGCACC 1000
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