| Tag | Content |
|---|
EnhancerAtlas ID | HS073-03421 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr12:110808490-110809080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr12:110808897-110808908 | CTGCAGCTGTT | - | 6.02 | | Myog | MA0500.1 | chr12:110808854-110808865 | GACAGCTGCAG | + | 6.62 | | TFAP2C | MA0524.2 | chr12:110808519-110808531 | TGCCCTGGGGCA | + | 6.44 | | TFAP2C | MA0524.2 | chr12:110808519-110808531 | TGCCCTGGGGCA | - | 7.22 | | Tcf12 | MA0521.1 | chr12:110808854-110808865 | GACAGCTGCAG | + | 6.14 | | Tcf12 | MA0521.1 | chr12:110808897-110808908 | CTGCAGCTGTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26768 | chr12:110806228-110813380 | Esophagus |
|
| | 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 |
| GH12I110370 | chr12 | 110807911 | 110810047 |
|
Enhancer Sequence | CGGGAGGTGG CAACTGAGGC CCCTCCTGCT GCCCTGGGGC AGGGAGGCTC CTGCAGAAAG 60
TGGAAAACCT TAGTAAGGCA CTTACCTCAA TGGCCCCTCC CAGCGCAGGG CTTCCCGGTG 120
ACCTGGCCAC AGCCGTGCCT GGAGGATGAG GTGAGGTTCA TGTGGAGTCT GGACTCACTG 180
CCTGTCGTCA GCAGGGAACG CAGGCCTGAG CACAACCCCA GAGAGCTGCT CACGGGGACA 240
GCTCACCTAA GCTCTGGGAA GCAGCTCCGC GCAGGCCCTG GCCTGCCACA GGTAAGCCAG 300
TGTAGGGCTG GGAACGCAGG AAGCCACAGG TGAGGCCTTT GGAGGCCGGT TCCTCCCACC 360
CACGGACAGC TGCAGAGTTA ACTCCCAAGG GCCCTCTGGG GTCAGGCCTG CAGCTGTTGG 420
GAACTTCGAG CTCCCCTCTC GCAGGTTTCT CAATACTTTT CCAGGGAACA CCTGCATAGA 480
ATAGGAAGTC AGGGTGGGAA GTGAAAGCTG CAGACCACTG GGCCTGGGCC AGGCCTCTGG 540
ATTCCAATAA AAGTTTGGTG CTGGGCCTGG GAACCTGCAT CGCTGAGATG 590
|
