| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:98446792-98446971 | Rare:46; Clinvar:1 | ||||
| chr10:99235957-99236242 | Common:5; Rare:62 | ||||
| chr10:99430523-99430965 | Common:4; Rare:119 | ||||
| chr10:99532773-99532959 | Common:4; Rare:36 | ||||
| chr10:99659244-99659591 | Common:2; Rare:88 | ||||
| chr10:99732028-99732351 | Rare:122; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:100185764-100186194 | Rare:144 | ||||
| chr10:100229553-100229672 | Rare:42 | ||||
| chr10:100267620-100267746 | Common:2; Rare:36 | ||||
| chr10:100286649-100286717 | Common:1; Rare:39 | ||||
| chr10:100346921-100347340 | Common:1; Rare:95 | ||||
| chr10:100912675-100913050 | Common:1; Rare:109 | ||||
| chr10:100913328-100913436 | Rare:30 | ||||
| chr10:100969241-100969570 | Common:3; Rare:81 | ||||
| chr10:100987429-100987613 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):2 |