Tag | Content |
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EnhancerAtlas ID | HS007-05152 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr14:77466490-77467380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr14:77466577-77466591 | CCCCTCTGGGCCCC | - | 6.36 |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I076996 | chr14 | 77462814 | 77467838 |
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Enhancer Sequence | GCTAGCAGAG CCACCACTAT GCCAGGTTTC ATGGGGCTCC GGCTGCTCAG GACTAGAGAG 60 GGTGTCTAAG CATCTGTGAG GTTTTCTCCC CTCTGGGCCC CTTGGGCCAG GAGGGAGGCA 120 CAGGGGTGGG TGGGGGCCAG CTGGGGCTGG GGGGAGCTAG TTGGGGGGAA TCAGCCTTTC 180 ATCTTGGCTG TGTGAAGCAA ACCCAACCCC TCCCCAGCCT GAAGCTGGCT GGCATTGGCA 240 TGCACCATAA ATCTCCAGGA TGCAGCTGTG ACTGGATTAT TTATAGCTCC AGTCTTACAT 300 CTCTAACTCG AAACTGTCAC ACAAAGGGAA AGGTAATGAA ATCTCACCTC TCCTGCCTGT 360 CCCTCAGTCC ACACCGCAGG GCCTTCCAGA GCCTGTGGCT GAAGGAGGGA GGAGAGGCCT 420 CCCCCCCTGC CGCCTCCCTC CCTTCCTGGC TCCCTCTGTC TTCTCCTCTG TCGTCACGCA 480 CACACTTCGC AGCGCTACGT TCCCTCTCAG ACACAGCCTC TCACGTTTTC TTTCTCTCTC 540 ACGCATACAT TTCCTCACAG ATGCAGACAT TTCTGTCCAG CCTCTTCCTC CCGCTCAGCT 600 CGCCCTGCCC GGGCCCCTCC TATCCCTGCA GACACACTTG CACACGCCTG CCCTTTTCCT 660 TCCACGCCAC CACTGTCTCC CTGCGTGGCT CACTCCCTTC CGCCTTGTTT GCCTCTTTGC 720 TTTGTCAATG AAGACGCTGC CACATTAATG AGCAGGCCTG TCCTCTGTGG AGGCACACCG 780 GCTCTTTGTC GCTCACTGGC AGAAGTGTCA GCTCACATTC ATCTTGCTCT GCCTGTAAGA 840 GTCCCACGGG CATTGCCTCC CCAAGTGGGA CCCATTTTGT GGCACGTGGC 890
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