| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100969010-100969637 | Common:8; Rare:234 | ||||
| chr10:100987100-100987632 | Common:4; Rare:335; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:100998080-100998392 | Common:2; Rare:130 | ||||
| chr10:100999633-100999894 | Common:1; Rare:144 | ||||
| chr10:101031093-101031305 | Common:2; Rare:93 | ||||
| chr10:101061686-101061999 | Rare:90 | ||||
| chr10:101588113-101588360 | Rare:211; Clinvar:2 | ||||
| chr10:101694844-101695005 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:101817960-101818310 | Common:1; Rare:111 | ||||
| chr10:101818357-101818817 | Common:2; Rare:235 | ||||
| chr10:102056088-102056390 | Common:3; Rare:136 | ||||
| chr10:102114938-102115115 | Common:4; Rare:105 | ||||
| chr10:102120416-102120720 | Common:2; Rare:194 | ||||
| chr10:102132776-102133126 | Common:1; Rare:95 | ||||
| chr10:102152112-102152433 | Common:3; Rare:110 |