| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100996965-100997144 | Common:2; Rare:51 | ||||
| chr10:100997771-100997877 | Common:1; Rare:23 | ||||
| chr10:100999190-100999379 | Common:3; Rare:34 | ||||
| chr10:100999579-100999857 | Common:1; Rare:79 | ||||
| chr10:101000316-101000392 | Rare:9 | ||||
| chr10:101061604-101061989 | Rare:63 | ||||
| chr10:101062611-101062711 | Common:1; Rare:36 | ||||
| chr10:101063014-101063368 | Rare:82 | ||||
| chr10:101063477-101063682 | Common:1; Rare:36 | ||||
| chr10:101353743-101354259 | Common:1; Rare:156 | ||||
| chr10:101354539-101354633 | Rare:27 | ||||
| chr10:101354648-101354666 | Rare:3 | ||||
| chr10:101588087-101588388 | Rare:129; Clinvar:1 | ||||
| chr10:101694648-101695370 | Common:3; Rare:150; Clinvar:3; Clinvar (benign):2 | ||||
| chr10:101783331-101783499 | Rare:73 |