| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99430569-99431001 | Common:4; Rare:105 | ||||
| chr10:99532755-99532962 | Common:4; Rare:40 | ||||
| chr10:99659247-99659562 | Common:1; Rare:79 | ||||
| chr10:99732063-99732335 | Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:100185895-100186198 | Rare:113 | ||||
| chr10:100229553-100229652 | Rare:31 | ||||
| chr10:100286649-100286750 | Common:2; Rare:50 | ||||
| chr10:100346929-100347380 | Common:1; Rare:102 | ||||
| chr10:100912751-100913009 | Common:1; Rare:79 | ||||
| chr10:100913335-100913359 | Rare:8 | ||||
| chr10:100969308-100969610 | Common:3; Rare:73 | ||||
| chr10:100980459-100980645 | Common:2; Rare:45 | ||||
| chr10:100987437-100987573 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100999678-100999930 | Common:1; Rare:74 | ||||
| chr10:101031076-101031534 | Common:1; Rare:106 |