| Tag | Content |
|---|
EnhancerAtlas ID | HS116-17156 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr19:33887650-33888800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr19:33887976-33887997 | GGCACTCCCCGAGGTCCTGCA | - | 6.11 | | RREB1 | MA0073.1 | chr19:33888501-33888521 | GGGTGGTAGGTGTGGGGGGG | - | 6.03 | | RREB1 | MA0073.1 | chr19:33888498-33888518 | TGTGGGTGGTAGGTGTGGGG | - | 6.47 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25205 | chr19:33887577-33889274 | Colon_Crypt_3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 33888059 | 33888360 | | chr19 | 33887919 | 33888334 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I033388 | chr19 | 33878998 | 33889454 |
|
Enhancer Sequence | GGGAGGCGAG GCTACAGGAG GCTCTGGGGC TTGCAGGCGG AGGGCATGGG GCCCTCAGTG 60
CTGGGGTCCT CTGGAGCTCC AGGGTGGCTG CAGGGACTGA GCCCGCGGGA CAGGGACAGC 120
TGTGCTGCTT CTAGGAACAG CCTTCCTGCT GTGGCTGTGC CAATGCAGAC CCTGACTCAG 180
GGCCACCCTG CCGGGCTCGC CCATCCGTCC CAGCAGCGCC TCCCCCCATT CCCCTCACCA 240
TGCATGCAGG GGTCTGCATG GGGTGGGCAG CCTGCCCCAA CACAGGAGCC GCGCTGAGCT 300
TGGATCCCAC CCAACCTCCC GTGCATGGCA CTCCCCGAGG TCCTGCAGCT GCTGGGCCTG 360
CCCTGCCACC CGCCTGTGGA CTCCCAGCCG CCAGGGTAGG GTCTCCGTCT GAGCGAGCGC 420
AGCCTCCTTC CTCGCCGACT GTGAATGACA GTGAGGAATG CTCCCCCACC AGCCCTAGGA 480
TCAGGGGCCA AGGCCTGCAT TCCTCAACCC CCCAGGGTCC TGACCATTCT TTCCTGCCTC 540
TCCTTTGGGC TTAGCTATGG GGTTTCCTGC TTTATTTACT CTCCCTGGAA GGTCACAGGA 600
TGCAGTCGGG CAGTCTCGGT GGGGTGTTTG TCTTGGCCCA GGAATTGAAC CCACGAACCC 660
AGGGCATTTC CGCTGGGACA AGGCAGGGGG CTGACCTGGC CACGGCCTCC TCGATGCTAC 720
GGGAGGCGAC CTGCCCCATC CGGAGGGCAG CTCTGTGGGC CCAGGGCCTG CCCCACGGGC 780
CTTCACTGTG TGTGATCCAG ATGGAGTCCG ACTCTGCCCT TGGGGGACAC CAATGCCACA 840
CAGCTCAGTG TGGGTGGTAG GTGTGGGGGG GCTGCTGGGG GGCTGCTCCA TTCCCTTACA 900
CAGGGATCCT CCAGACCCCA GGCTGGGTCT GGGCAGCAAA GCCCAGTGGT GGGTGGGAGC 960
GGGGCTGGGG GAGGACCTGC CTCCCATGGT CTGAGATGAG CCTAGCTGGA TTTGGCCTTG 1020
TGGCCCCAGA CACCCCTGCC AGGCCTGAGG CCTGTGCCTG CCCCAAGAGT CAGCATGAAC 1080
CAGGCAGCAC CACGGGATGG GAGACCCAGC TCAGGCCTTT CTCAGTGCCA CATGGGGCCT 1140
GGGGACTTGC 1150
|
