| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68956570-68956676 | Rare:20 | ||||
| chr10:68989038-68989091 | Rare:14; Clinvar (pathogenic):1 | ||||
| chr10:69087990-69088234 | Rare:53 | ||||
| chr10:69179907-69180341 | Common:3; Rare:144 | ||||
| chr10:69318594-69318922 | Common:4; Rare:96 | ||||
| chr10:69451323-69451581 | Common:2; Rare:73 | ||||
| chr10:70132686-70132944 | Common:2; Rare:71 | ||||
| chr10:70146189-70146296 | Common:2; Rare:43 | ||||
| chr10:70146613-70146870 | Common:1; Rare:74 | ||||
| chr10:70170424-70170767 | Common:4; Rare:107 | ||||
| chr10:70233266-70233612 | Common:6; Rare:121; Clinvar (benign):1 | ||||
| chr10:70403990-70404164 | Rare:64 | ||||
| chr10:70478640-70478998 | Rare:119 | ||||
| chr10:70815797-70816021 | Rare:89 | ||||
| chr10:70888524-70888643 | Common:1; Rare:42; Clinvar:5; Clinvar (benign):1 |