| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73625996-73626152 | Rare:36 | ||||
| chr10:73743891-73744424 | Common:2; Rare:131 | ||||
| chr10:73781942-73782073 | Common:1; Rare:41 | ||||
| chr10:74151032-74151262 | Common:1; Rare:61 | ||||
| chr10:74176449-74176558 | Rare:23 | ||||
| chr10:75111282-75111699 | Common:1; Rare:113 | ||||
| chr10:80078611-80078677 | Rare:19 | ||||
| chr10:80079012-80079282 | Common:2; Rare:108 | ||||
| chr10:80157673-80158004 | Common:4; Rare:100 | ||||
| chr10:84139282-84139586 | Common:3; Rare:79 | ||||
| chr10:86521739-86521975 | Rare:81 | ||||
| chr10:87095003-87095239 | Common:1; Rare:52 | ||||
| chr10:87504818-87504918 | Common:1; Rare:44 | ||||
| chr10:87818162-87818349 | Common:1; Rare:72 | ||||
| chr10:87863328-87863659 | Common:2; Rare:108; Clinvar:66; Clinvar (benign):7 |