Tag | Content |
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EnhancerAtlas ID | HS010-01492 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr14:77466740-77467570 |
| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_23394 | chr14:77466591-77467245 | Colon_Crypt_1 | SE_23908 | chr14:77466836-77467311 | Colon_Crypt_2 | SE_26622 | chr14:77466561-77467537 | Esophagus | SE_27835 | chr14:77466651-77467464 | Fetal_Intestine | SE_31397 | chr14:77464388-77467947 | Gastric | SE_41587 | chr14:77466618-77467621 | LNCaP | SE_42117 | chr14:77466676-77467710 | Lung | SE_48172 | chr14:77466511-77467551 | Psoas_Muscle | SE_51190 | chr14:77466291-77468033 | Skeletal_Muscle | SE_65357 | chr14:77466293-77467871 | Pancreatic_islets | SE_68819 | chr14:77466615-77468062 | H9 |
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| 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 |
GH14I076996 | chr14 | 77462814 | 77467838 |
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Enhancer Sequence | ATCTCCAGGA TGCAGCTGTG ACTGGATTAT TTATAGCTCC AGTCTTACAT CTCTAACTCG 60 AAACTGTCAC ACAAAGGGAA AGGTAATGAA ATCTCACCTC TCCTGCCTGT CCCTCAGTCC 120 ACACCGCAGG GCCTTCCAGA GCCTGTGGCT GAAGGAGGGA GGAGAGGCCT CCCCCCCTGC 180 CGCCTCCCTC CCTTCCTGGC TCCCTCTGTC TTCTCCTCTG TCGTCACGCA CACACTTCGC 240 AGCGCTACGT TCCCTCTCAG ACACAGCCTC TCACGTTTTC TTTCTCTCTC ACGCATACAT 300 TTCCTCACAG ATGCAGACAT TTCTGTCCAG CCTCTTCCTC CCGCTCAGCT CGCCCTGCCC 360 GGGCCCCTCC TATCCCTGCA GACACACTTG CACACGCCTG CCCTTTTCCT TCCACGCCAC 420 CACTGTCTCC CTGCGTGGCT CACTCCCTTC CGCCTTGTTT GCCTCTTTGC TTTGTCAATG 480 AAGACGCTGC CACATTAATG AGCAGGCCTG TCCTCTGTGG AGGCACACCG GCTCTTTGTC 540 GCTCACTGGC AGAAGTGTCA GCTCACATTC ATCTTGCTCT GCCTGTAAGA GTCCCACGGG 600 CATTGCCTCC CCAAGTGGGA CCCATTTTGT GGCACGTGGC CCGGACGACA CGTATCCCTG 660 GGCTTGACAT ACACAGACAC ACAGGAAACA TTGGCCATGG GACATGCCTC TCCCCCTGCA 720 GTGAGGAGCA TCTAAGGATG CGCTCTGCAA ATTCCACGAA AGGCCCCGGG TGCGGTATTT 780 CATGGTGCAG AGGTGAAGTT CCTCCTCCCT CCTGTTTCGT TGTCTCGCAG 830
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