Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151059232-151059658 | Rare:93 | ||||
chr1:151165889-151166157 | Common:3; Rare:77 | ||||
chr1:151281241-151281529 | Common:3; Rare:90 | ||||
chr1:151281941-151282309 | Rare:106 | ||||
chr1:151346873-151347056 | Rare:48 | ||||
chr1:151347188-151347534 | Rare:81 | ||||
chr1:151399472-151399581 | Common:1; Rare:32; Clinvar (pathogenic):1 | ||||
chr1:151790480-151790833 | Common:2; Rare:76 | ||||
chr1:151992453-151992837 | Common:3; Rare:72 | ||||
chr1:151993782-151994010 | Common:3; Rare:84 | ||||
chr1:152036911-152037122 | Common:2; Rare:57 | ||||
chr1:152048165-152048395 | Rare:44 | ||||
chr1:153357769-153357909 | Rare:25 | ||||
chr1:153375584-153375632 | Rare:4 | ||||
chr1:153545733-153545924 | Rare:33 |