| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:95656632-95656762 | Common:1; Rare:46; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:95907756-95907940 | Common:2; Rare:51 | ||||
| chr10:96129709-96129737 | Rare:5 | ||||
| chr10:96513748-96514080 | Common:4; Rare:69 | ||||
| chr10:97425902-97426299 | Common:15; Rare:183 | ||||
| chr10:97445969-97446229 | Common:1; Rare:69 | ||||
| chr10:97498382-97498550 | Common:2; Rare:69 | ||||
| chr10:97498694-97498989 | Common:2; Rare:86 | ||||
| chr10:97736994-97737159 | Common:1; Rare:53 | ||||
| chr10:98268193-98268433 | Common:2; Rare:61 | ||||
| chr10:99430609-99430940 | Common:3; Rare:76 | ||||
| chr10:99732056-99732330 | Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:100185938-100186182 | Rare:95 | ||||
| chr10:100229553-100229668 | Rare:40 | ||||
| chr10:100267589-100267733 | Common:3; Rare:50 |