| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99619915-99620120 | Common:1; Rare:40 | ||||
| chr10:99620370-99621139 | Common:3; Rare:212 | ||||
| chr10:99659236-99659566 | Common:1; Rare:84 | ||||
| chr10:99732005-99732506 | Common:3; Rare:185; Clinvar:7; Clinvar (benign):2 | ||||
| chr10:99732526-99732771 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:99732866-99732903 | Rare:7 | ||||
| chr10:99913755-99913792 | Rare:6 | ||||
| chr10:99913932-99914203 | Rare:77 | ||||
| chr10:100009445-100009509 | Common:1; Rare:9 | ||||
| chr10:100009660-100009714 | Rare:9 | ||||
| chr10:100009867-100010005 | Common:1; Rare:45 | ||||
| chr10:100010039-100010217 | Rare:46 | ||||
| chr10:100185581-100185656 | Rare:27 | ||||
| chr10:100185866-100186266 | Common:1; Rare:135 | ||||
| chr10:100186303-100186421 | Common:1; Rare:18 |