| Tag | Content |
|---|
EnhancerAtlas ID | HS136-06179 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr14:77466540-77467550 |
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 | GACTAGAGAG GGTGTCTAAG CATCTGTGAG GTTTTCTCCC CTCTGGGCCC CTTGGGCCAG 60
GAGGGAGGCA CAGGGGTGGG TGGGGGCCAG CTGGGGCTGG GGGGAGCTAG TTGGGGGGAA 120
TCAGCCTTTC ATCTTGGCTG TGTGAAGCAA ACCCAACCCC TCCCCAGCCT GAAGCTGGCT 180
GGCATTGGCA TGCACCATAA ATCTCCAGGA TGCAGCTGTG ACTGGATTAT TTATAGCTCC 240
AGTCTTACAT CTCTAACTCG AAACTGTCAC ACAAAGGGAA AGGTAATGAA ATCTCACCTC 300
TCCTGCCTGT CCCTCAGTCC ACACCGCAGG GCCTTCCAGA GCCTGTGGCT GAAGGAGGGA 360
GGAGAGGCCT CCCCCCCTGC CGCCTCCCTC CCTTCCTGGC TCCCTCTGTC TTCTCCTCTG 420
TCGTCACGCA CACACTTCGC AGCGCTACGT TCCCTCTCAG ACACAGCCTC TCACGTTTTC 480
TTTCTCTCTC ACGCATACAT TTCCTCACAG ATGCAGACAT TTCTGTCCAG CCTCTTCCTC 540
CCGCTCAGCT CGCCCTGCCC GGGCCCCTCC TATCCCTGCA GACACACTTG CACACGCCTG 600
CCCTTTTCCT TCCACGCCAC CACTGTCTCC CTGCGTGGCT CACTCCCTTC CGCCTTGTTT 660
GCCTCTTTGC TTTGTCAATG AAGACGCTGC CACATTAATG AGCAGGCCTG TCCTCTGTGG 720
AGGCACACCG GCTCTTTGTC GCTCACTGGC AGAAGTGTCA GCTCACATTC ATCTTGCTCT 780
GCCTGTAAGA GTCCCACGGG CATTGCCTCC CCAAGTGGGA CCCATTTTGT GGCACGTGGC 840
CCGGACGACA CGTATCCCTG GGCTTGACAT ACACAGACAC ACAGGAAACA TTGGCCATGG 900
GACATGCCTC TCCCCCTGCA GTGAGGAGCA TCTAAGGATG CGCTCTGCAA ATTCCACGAA 960
AGGCCCCGGG TGCGGTATTT CATGGTGCAG AGGTGAAGTT CCTCCTCCCT 1010
|
