Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151254624-151254851 | Common:1; Rare:61 | ||||
chr1:151281241-151281554 | Common:4; Rare:101 | ||||
chr1:151281853-151282327 | Rare:130 | ||||
chr1:151327584-151327808 | Common:2; Rare:45 | ||||
chr1:151346827-151347083 | Rare:71 | ||||
chr1:151347220-151347428 | Rare:48 | ||||
chr1:151399351-151399596 | Common:2; Rare:66; Clinvar (pathogenic):1 | ||||
chr1:151511125-151511406 | Common:3; Rare:64 | ||||
chr1:151540137-151540361 | Common:1; Rare:74 | ||||
chr1:151710296-151710533 | Rare:66 | ||||
chr1:151715962-151716452 | Common:5; Rare:89 | ||||
chr1:151716543-151717246 | Common:3; Rare:172 | ||||
chr1:151721450-151721595 | Rare:49 | ||||
chr1:151763172-151763570 | Common:2; Rare:156 | ||||
chr1:151790426-151790876 | Common:3; Rare:111 |