| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:7818360-7818538 | Common:1; Rare:44 | ||||
| chr10:12043126-12043427 | Common:2; Rare:86 | ||||
| chr10:12068656-12069027 | Common:2; Rare:131 | ||||
| chr10:12129456-12129726 | Rare:109 | ||||
| chr10:12195781-12195974 | Rare:47 | ||||
| chr10:13099966-13100205 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:13161323-13161599 | Common:1; Rare:74 | ||||
| chr10:13300037-13300153 | Rare:46; Clinvar:1 | ||||
| chr10:13348001-13348438 | Rare:139 | ||||
| chr10:13707550-13707651 | Rare:21 | ||||
| chr10:14838029-14838386 | Common:2; Rare:100 | ||||
| chr10:14878604-14878901 | Common:2; Rare:95 | ||||
| chr10:14953994-14954195 | Rare:71 | ||||
| chr10:15097306-15097409 | Common:1; Rare:48 | ||||
| chr10:15860426-15860614 | Rare:50 |