| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:98832760-98832783 | Common:1; Rare:2 | ||||
| chr3:98843493-98843619 | Rare:25 | ||||
| chr3:98845814-98846121 | Common:1; Rare:57 | ||||
| chr3:98909514-98909775 | Common:6; Rare:52 | ||||
| chr3:98909960-98910076 | Common:1; Rare:23 | ||||
| chr3:98966895-98967302 | Common:1; Rare:81 | ||||
| chr3:99948393-99948572 | Common:1; Rare:32 | ||||
| chr3:100362526-100362626 | Common:1; Rare:19 | ||||
| chr3:100744563-100744965 | Common:3; Rare:92; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:100748122-100748169 | Rare:12 | ||||
| chr3:101676243-101676481 | Common:2; Rare:78 | ||||
| chr3:104445415-104445432 | Rare:4 | ||||
| chr3:105402089-105402157 | Rare:8 | ||||
| chr3:105403974-105404425 | Common:2; Rare:86 | ||||
| chr3:105404938-105405218 | Common:1; Rare:62 |