| Tag | Content |
|---|
EnhancerAtlas ID | HS145-06174 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr12:110808510-110809100 |
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 | CCCTCCTGCT GCCCTGGGGC AGGGAGGCTC CTGCAGAAAG TGGAAAACCT TAGTAAGGCA 60
CTTACCTCAA TGGCCCCTCC CAGCGCAGGG CTTCCCGGTG ACCTGGCCAC AGCCGTGCCT 120
GGAGGATGAG GTGAGGTTCA TGTGGAGTCT GGACTCACTG CCTGTCGTCA GCAGGGAACG 180
CAGGCCTGAG CACAACCCCA GAGAGCTGCT CACGGGGACA GCTCACCTAA GCTCTGGGAA 240
GCAGCTCCGC GCAGGCCCTG GCCTGCCACA GGTAAGCCAG TGTAGGGCTG GGAACGCAGG 300
AAGCCACAGG TGAGGCCTTT GGAGGCCGGT TCCTCCCACC CACGGACAGC TGCAGAGTTA 360
ACTCCCAAGG GCCCTCTGGG GTCAGGCCTG CAGCTGTTGG GAACTTCGAG CTCCCCTCTC 420
GCAGGTTTCT CAATACTTTT CCAGGGAACA CCTGCATAGA ATAGGAAGTC AGGGTGGGAA 480
GTGAAAGCTG CAGACCACTG GGCCTGGGCC AGGCCTCTGG ATTCCAATAA AAGTTTGGTG 540
CTGGGCCTGG GAACCTGCAT CGCTGAGATG CATGCTCTAG TTTGGGGATT 590
|
