| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112584265-112584719 | Common:2; Rare:133 | ||||
| chr2:112584757-112585000 | Common:1; Rare:50 | ||||
| chr2:112645255-112645447 | Rare:43 | ||||
| chr2:112645474-112645535 | Common:1; Rare:11 | ||||
| chr2:112645556-112646066 | Common:3; Rare:173 | ||||
| chr2:112646249-112646386 | Common:1; Rare:47 | ||||
| chr2:112764113-112764188 | Common:1; Rare:23 | ||||
| chr2:112764525-112764906 | Common:4; Rare:133; Clinvar (pathogenic):1 | ||||
| chr2:113157111-113157206 | Rare:25 | ||||
| chr2:113157252-113157457 | Common:3; Rare:50 | ||||
| chr2:113173587-113174047 | Common:3; Rare:82 | ||||
| chr2:113174178-113174314 | Common:1; Rare:16 | ||||
| chr2:113626607-113626811 | Common:3; Rare:35 | ||||
| chr2:113627078-113627304 | Common:3; Rare:64 | ||||
| chr2:113756172-113756281 | Common:1; Rare:28 |