| Tag | Content |
|---|
EnhancerAtlas ID | HS044-04369 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr14:77466240-77467900 |
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 | CAATTCTCCT GCCTCAGCCT CCCGAGTTGC TGGAATTACA GGCGCACGCC ACCATGCTCA 60
GCTGACTTTT GTATTTTTAG TAGAGACGGG TTTTCACCAT GTTGGCCAGG CTGATCTCGA 120
ACTCCTGACC TCAAGTGATC CTCCCTCCTT GGCCTCCCAA AGTGCTGGGA TTACAGGCAT 180
GAGGCAGCGC GCCCGCCCTG GTAAGGCACC TTCTGCCCAC CTTGCTCCCC CTGCCCCATT 240
GGTCTCCCCA GCTAGCAGAG CCACCACTAT GCCAGGTTTC ATGGGGCTCC GGCTGCTCAG 300
GACTAGAGAG GGTGTCTAAG CATCTGTGAG GTTTTCTCCC CTCTGGGCCC CTTGGGCCAG 360
GAGGGAGGCA CAGGGGTGGG TGGGGGCCAG CTGGGGCTGG GGGGAGCTAG TTGGGGGGAA 420
TCAGCCTTTC ATCTTGGCTG TGTGAAGCAA ACCCAACCCC TCCCCAGCCT GAAGCTGGCT 480
GGCATTGGCA TGCACCATAA ATCTCCAGGA TGCAGCTGTG ACTGGATTAT TTATAGCTCC 540
AGTCTTACAT CTCTAACTCG AAACTGTCAC ACAAAGGGAA AGGTAATGAA ATCTCACCTC 600
TCCTGCCTGT CCCTCAGTCC ACACCGCAGG GCCTTCCAGA GCCTGTGGCT GAAGGAGGGA 660
GGAGAGGCCT CCCCCCCTGC CGCCTCCCTC CCTTCCTGGC TCCCTCTGTC TTCTCCTCTG 720
TCGTCACGCA CACACTTCGC AGCGCTACGT TCCCTCTCAG ACACAGCCTC TCACGTTTTC 780
TTTCTCTCTC ACGCATACAT TTCCTCACAG ATGCAGACAT TTCTGTCCAG CCTCTTCCTC 840
CCGCTCAGCT CGCCCTGCCC GGGCCCCTCC TATCCCTGCA GACACACTTG CACACGCCTG 900
CCCTTTTCCT TCCACGCCAC CACTGTCTCC CTGCGTGGCT CACTCCCTTC CGCCTTGTTT 960
GCCTCTTTGC TTTGTCAATG AAGACGCTGC CACATTAATG AGCAGGCCTG TCCTCTGTGG 1020
AGGCACACCG GCTCTTTGTC GCTCACTGGC AGAAGTGTCA GCTCACATTC ATCTTGCTCT 1080
GCCTGTAAGA GTCCCACGGG CATTGCCTCC CCAAGTGGGA CCCATTTTGT GGCACGTGGC 1140
CCGGACGACA CGTATCCCTG GGCTTGACAT ACACAGACAC ACAGGAAACA TTGGCCATGG 1200
GACATGCCTC TCCCCCTGCA GTGAGGAGCA TCTAAGGATG CGCTCTGCAA ATTCCACGAA 1260
AGGCCCCGGG TGCGGTATTT CATGGTGCAG AGGTGAAGTT CCTCCTCCCT CCTGTTTCGT 1320
TGTCTCGCAG TTTTCTACGG GCCAGTCCCT CTGTTACCCC ATCCCACAGG CGCCAATGGA 1380
AACTCTGAGC CCCATGCAAG CTCCCATGGA GACCCAAGGC CCAGCCTCTC TCCCTGCCCA 1440
GCCCTCCACC CCCAGGCCCG CAATCATCAG AAAGCAGCAC TTCCCACTGC AGCCCTGCCT 1500
TGACGTGGCC CACAACTCAC TCCATCCAGA CAGTCAGGGG GGTAGGCAGT GTGTATTTGT 1560
GTGTGTGTGT ATGTGTGTGC GCGCACTTCT TGTGCTGAAT GAGTGGTATT CACGAACAAT 1620
GGCAGCTTAC CCTGGGCTGA CGGTGGGGTT GGGCCTGGGG 1660
|
