| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68721475-68721553 | Rare:25 | ||||
| chr10:68901049-68901386 | Common:3; Rare:133 | ||||
| chr10:68956066-68956440 | Common:3; Rare:113 | ||||
| chr10:69087986-69088149 | Rare:33 | ||||
| chr10:69179898-69180315 | Common:3; Rare:135 | ||||
| chr10:69494748-69495014 | Common:3; Rare:58 | ||||
| chr10:69630045-69630293 | Common:2; Rare:68 | ||||
| chr10:70052710-70052877 | Rare:36 | ||||
| chr10:70132750-70132926 | Rare:47 | ||||
| chr10:70146616-70146869 | Common:1; Rare:73 | ||||
| chr10:70170454-70170742 | Common:3; Rare:91 | ||||
| chr10:70233338-70233566 | Common:5; Rare:82 | ||||
| chr10:70403983-70404179 | Rare:73 | ||||
| chr10:70888524-70888653 | Common:1; Rare:44; Clinvar:5; Clinvar (benign):1 | ||||
| chr10:71319101-71319291 | Common:4; Rare:59; Clinvar:2; Clinvar (benign):1 |