| Tag | Content |
|---|
EnhancerAtlas ID | HS073-04198 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr14:77466430-77467540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr14:77466577-77466591 | CCCCTCTGGGCCCC | - | 6.36 |
|
| | 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 | GCCCGCCCTG GTAAGGCACC TTCTGCCCAC CTTGCTCCCC CTGCCCCATT GGTCTCCCCA 60
GCTAGCAGAG CCACCACTAT GCCAGGTTTC ATGGGGCTCC GGCTGCTCAG GACTAGAGAG 120
GGTGTCTAAG CATCTGTGAG GTTTTCTCCC CTCTGGGCCC CTTGGGCCAG GAGGGAGGCA 180
CAGGGGTGGG TGGGGGCCAG CTGGGGCTGG GGGGAGCTAG TTGGGGGGAA TCAGCCTTTC 240
ATCTTGGCTG TGTGAAGCAA ACCCAACCCC TCCCCAGCCT GAAGCTGGCT GGCATTGGCA 300
TGCACCATAA ATCTCCAGGA TGCAGCTGTG ACTGGATTAT TTATAGCTCC AGTCTTACAT 360
CTCTAACTCG AAACTGTCAC ACAAAGGGAA AGGTAATGAA ATCTCACCTC TCCTGCCTGT 420
CCCTCAGTCC ACACCGCAGG GCCTTCCAGA GCCTGTGGCT GAAGGAGGGA GGAGAGGCCT 480
CCCCCCCTGC CGCCTCCCTC CCTTCCTGGC TCCCTCTGTC TTCTCCTCTG TCGTCACGCA 540
CACACTTCGC AGCGCTACGT TCCCTCTCAG ACACAGCCTC TCACGTTTTC TTTCTCTCTC 600
ACGCATACAT TTCCTCACAG ATGCAGACAT TTCTGTCCAG CCTCTTCCTC CCGCTCAGCT 660
CGCCCTGCCC GGGCCCCTCC TATCCCTGCA GACACACTTG CACACGCCTG CCCTTTTCCT 720
TCCACGCCAC CACTGTCTCC CTGCGTGGCT CACTCCCTTC CGCCTTGTTT GCCTCTTTGC 780
TTTGTCAATG AAGACGCTGC CACATTAATG AGCAGGCCTG TCCTCTGTGG AGGCACACCG 840
GCTCTTTGTC GCTCACTGGC AGAAGTGTCA GCTCACATTC ATCTTGCTCT GCCTGTAAGA 900
GTCCCACGGG CATTGCCTCC CCAAGTGGGA CCCATTTTGT GGCACGTGGC CCGGACGACA 960
CGTATCCCTG GGCTTGACAT ACACAGACAC ACAGGAAACA TTGGCCATGG GACATGCCTC 1020
TCCCCCTGCA GTGAGGAGCA TCTAAGGATG CGCTCTGCAA ATTCCACGAA AGGCCCCGGG 1080
TGCGGTATTT CATGGTGCAG AGGTGAAGTT 1110
|
