| Tag | Content |
|---|
EnhancerAtlas ID | HS153-02024 |
Organism | Homo sapiens |
Tissue/cell | Osteobl |
Coordinate | chr19:1124020-1125030 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:1124089-1124108 | TGGCCACCAGAGGGAGGCT | + | 6.57 | | PLAG1 | MA0163.1 | chr19:1124427-1124441 | GAGGCCCTCGGGGG | + | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_68758 | chr19:1123276-1124449 | 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 |
| GH19I001122 | chr19 | 1122862 | 1124147 |
|
Enhancer Sequence | GCTGGAAGGG GAGCAGGATG TCAGCCCGGG CCAGACGGGA CAGGTCACAG CTGGTGGGCC 60
CTCGCAGCCT GGCCACCAGA GGGAGGCTCC CCACTGCCCC GTCCTCGCCT CCCCATCCTC 120
GCTCCCCAGG GCCCTGGGTC TTGCTCTCCT GCTGTTCTCA GGGTGACCCT GGTGCCTCCC 180
AAGCCTCCCC AGTGGGCACC TCCCTGGGGC CTAAGGCTCG CTCCTCCTGG CCAGCACCTG 240
GCTGCCTTCT CACTGATGGC CAGTGTGCCT GCCTGGAGTG CCCGGGAGGA AGGTGCCCGG 300
CTAGTTCTGA CAGACAACAC AGCTTGGTCC CGCGGGAGCT GCCAGGAAGG CTGTGGACAG 360
GGGTCTGACA GGAGAGACCC ACTGTGTGCC AGCCCCATGC AGTGCAGGAG GCCCTCGGGG 420
GCCTGGGAGA CAAGGGGTTG GGAGCTCCCT GTCGAGGGGG AAGAGGAGAC AGAGGCAGTG 480
GGGGCGGGCG GGCCTGGGCC TTGTCCCTCA CCCGATGGCT CCCAGCACAC AGGGTGGGTG 540
GCCCAGGGCA GCCCTGCACT CTCCAAGAAC CCCCGTGGGT GCAGTCCCTG AGGCCCCTCG 600
AGGGCAGCAC CTCCTCTGTG AGAGATGGGG CAAGGATGCC TGCCACTGTA GTGACCAGAG 660
AACACATCCC ACTGCGGCCC CACCCTGGGG AGAAGGACTG CCCGGAGCCT CATGCAGATT 720
CACCAGGGTG GGCAGTGACA CTGTCCTCGG GGAGCTGACC CCAGGCCTTG GCAGACAGGT 780
GTGCTGGGCC TCTGGATGAG TCTGTGGCCC ACCCAGGGGT CTCCGAACTG ACTGGGCGTG 840
TAAAGCCTGT GAACGGGTGG GTCGGGGGGT GGTGTGGCCC GTCGTCATGC CCACTGTCCA 900
GACGCCAACA CTGAGACAGT GTGGACCCCG GGACGGATGG CTGGGGGATG GTAGGGTCCA 960
AACTAGGGTC TGTGTGATTC TGGAATATAT CCACTCTTAA AAAGCAAAAA 1010
|
