Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6485437-6485486 | Common:1; Rare:13 | ||||
chr1:6490503-6490691 | Rare:45 | ||||
chr1:6554475-6554636 | Common:3; Rare:59 | ||||
chr1:6579803-6580057 | Common:4; Rare:84 | ||||
chr1:6602857-6602976 | Common:1; Rare:49 | ||||
chr1:6613453-6613780 | Common:2; Rare:117 | ||||
chr1:6784953-6785340 | Common:1; Rare:124 | ||||
chr1:7771106-7771386 | Common:4; Rare:116 | ||||
chr1:7784053-7784371 | Rare:134 | ||||
chr1:7961446-7961791 | Common:4; Rare:119; Clinvar:3; Clinvar (benign):3 | ||||
chr1:8026291-8026428 | Rare:58 | ||||
chr1:8423700-8423898 | Common:1; Rare:90 | ||||
chr1:8424240-8424273 | Rare:8 | ||||
chr1:8703075-8703307 | Common:1; Rare:84 | ||||
chr1:8816766-8816966 | Rare:39 |