| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68901232-68901566 | Common:2; Rare:145 | ||||
| chr10:68901614-68901683 | Rare:19 | ||||
| chr10:68955545-68955713 | Common:2; Rare:33 | ||||
| chr10:68955726-68955985 | Common:1; Rare:51 | ||||
| chr10:68955990-68956462 | Common:3; Rare:136 | ||||
| chr10:68956486-68956718 | Common:1; Rare:51 | ||||
| chr10:68956731-68957174 | Common:4; Rare:83 | ||||
| chr10:68988668-68988963 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):4 | ||||
| chr10:68989007-68989192 | Common:1; Rare:54; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:68989201-68989308 | Rare:44 | ||||
| chr10:69123354-69123538 | Common:1; Rare:37 | ||||
| chr10:69123643-69123782 | Rare:23 | ||||
| chr10:69123800-69124290 | Common:4; Rare:164 | ||||
| chr10:69124385-69124589 | Common:2; Rare:55 | ||||
| chr10:69124706-69125013 | Common:4; Rare:65 |