Tag | Content |
---|
EnhancerAtlas ID | HS060-10596 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr14:77466260-77467840 |
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 | CCCGAGTTGC TGGAATTACA GGCGCACGCC ACCATGCTCA GCTGACTTTT GTATTTTTAG 60 TAGAGACGGG TTTTCACCAT GTTGGCCAGG CTGATCTCGA ACTCCTGACC TCAAGTGATC 120 CTCCCTCCTT GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGGCAGCGC GCCCGCCCTG 180 GTAAGGCACC TTCTGCCCAC CTTGCTCCCC CTGCCCCATT GGTCTCCCCA GCTAGCAGAG 240 CCACCACTAT GCCAGGTTTC ATGGGGCTCC GGCTGCTCAG GACTAGAGAG GGTGTCTAAG 300 CATCTGTGAG GTTTTCTCCC CTCTGGGCCC CTTGGGCCAG GAGGGAGGCA CAGGGGTGGG 360 TGGGGGCCAG CTGGGGCTGG GGGGAGCTAG TTGGGGGGAA TCAGCCTTTC ATCTTGGCTG 420 TGTGAAGCAA ACCCAACCCC TCCCCAGCCT GAAGCTGGCT GGCATTGGCA TGCACCATAA 480 ATCTCCAGGA TGCAGCTGTG ACTGGATTAT TTATAGCTCC AGTCTTACAT CTCTAACTCG 540 AAACTGTCAC ACAAAGGGAA AGGTAATGAA ATCTCACCTC TCCTGCCTGT CCCTCAGTCC 600 ACACCGCAGG GCCTTCCAGA GCCTGTGGCT GAAGGAGGGA GGAGAGGCCT CCCCCCCTGC 660 CGCCTCCCTC CCTTCCTGGC TCCCTCTGTC TTCTCCTCTG TCGTCACGCA CACACTTCGC 720 AGCGCTACGT TCCCTCTCAG ACACAGCCTC TCACGTTTTC TTTCTCTCTC ACGCATACAT 780 TTCCTCACAG ATGCAGACAT TTCTGTCCAG CCTCTTCCTC CCGCTCAGCT CGCCCTGCCC 840 GGGCCCCTCC TATCCCTGCA GACACACTTG CACACGCCTG CCCTTTTCCT TCCACGCCAC 900 CACTGTCTCC CTGCGTGGCT CACTCCCTTC CGCCTTGTTT GCCTCTTTGC TTTGTCAATG 960 AAGACGCTGC CACATTAATG AGCAGGCCTG TCCTCTGTGG AGGCACACCG GCTCTTTGTC 1020 GCTCACTGGC AGAAGTGTCA GCTCACATTC ATCTTGCTCT GCCTGTAAGA GTCCCACGGG 1080 CATTGCCTCC CCAAGTGGGA CCCATTTTGT GGCACGTGGC CCGGACGACA CGTATCCCTG 1140 GGCTTGACAT ACACAGACAC ACAGGAAACA TTGGCCATGG GACATGCCTC TCCCCCTGCA 1200 GTGAGGAGCA TCTAAGGATG CGCTCTGCAA ATTCCACGAA AGGCCCCGGG TGCGGTATTT 1260 CATGGTGCAG AGGTGAAGTT CCTCCTCCCT CCTGTTTCGT TGTCTCGCAG TTTTCTACGG 1320 GCCAGTCCCT CTGTTACCCC ATCCCACAGG CGCCAATGGA AACTCTGAGC CCCATGCAAG 1380 CTCCCATGGA GACCCAAGGC CCAGCCTCTC TCCCTGCCCA GCCCTCCACC CCCAGGCCCG 1440 CAATCATCAG AAAGCAGCAC TTCCCACTGC AGCCCTGCCT TGACGTGGCC CACAACTCAC 1500 TCCATCCAGA CAGTCAGGGG GGTAGGCAGT GTGTATTTGT GTGTGTGTGT ATGTGTGTGC 1560 GCGCACTTCT TGTGCTGAAT 1580
|