| Tag | Content |
|---|
EnhancerAtlas ID | HS052-11910 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr14:77466640-77467740 |
| | 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 |
|
| | 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 |
|
Enhancer Sequence | GGGGAGCTAG TTGGGGGGAA TCAGCCTTTC ATCTTGGCTG TGTGAAGCAA ACCCAACCCC 60
TCCCCAGCCT GAAGCTGGCT GGCATTGGCA TGCACCATAA ATCTCCAGGA TGCAGCTGTG 120
ACTGGATTAT TTATAGCTCC AGTCTTACAT CTCTAACTCG AAACTGTCAC ACAAAGGGAA 180
AGGTAATGAA ATCTCACCTC TCCTGCCTGT CCCTCAGTCC ACACCGCAGG GCCTTCCAGA 240
GCCTGTGGCT GAAGGAGGGA GGAGAGGCCT CCCCCCCTGC CGCCTCCCTC CCTTCCTGGC 300
TCCCTCTGTC TTCTCCTCTG TCGTCACGCA CACACTTCGC AGCGCTACGT TCCCTCTCAG 360
ACACAGCCTC TCACGTTTTC TTTCTCTCTC ACGCATACAT TTCCTCACAG ATGCAGACAT 420
TTCTGTCCAG CCTCTTCCTC CCGCTCAGCT CGCCCTGCCC GGGCCCCTCC TATCCCTGCA 480
GACACACTTG CACACGCCTG CCCTTTTCCT TCCACGCCAC CACTGTCTCC CTGCGTGGCT 540
CACTCCCTTC CGCCTTGTTT GCCTCTTTGC TTTGTCAATG AAGACGCTGC CACATTAATG 600
AGCAGGCCTG TCCTCTGTGG AGGCACACCG GCTCTTTGTC GCTCACTGGC AGAAGTGTCA 660
GCTCACATTC ATCTTGCTCT GCCTGTAAGA GTCCCACGGG CATTGCCTCC CCAAGTGGGA 720
CCCATTTTGT GGCACGTGGC CCGGACGACA CGTATCCCTG GGCTTGACAT ACACAGACAC 780
ACAGGAAACA TTGGCCATGG GACATGCCTC TCCCCCTGCA GTGAGGAGCA TCTAAGGATG 840
CGCTCTGCAA ATTCCACGAA AGGCCCCGGG TGCGGTATTT CATGGTGCAG AGGTGAAGTT 900
CCTCCTCCCT CCTGTTTCGT TGTCTCGCAG TTTTCTACGG GCCAGTCCCT CTGTTACCCC 960
ATCCCACAGG CGCCAATGGA AACTCTGAGC CCCATGCAAG CTCCCATGGA GACCCAAGGC 1020
CCAGCCTCTC TCCCTGCCCA GCCCTCCACC CCCAGGCCCG CAATCATCAG AAAGCAGCAC 1080
TTCCCACTGC AGCCCTGCCT 1100
|
