| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13001599-13001999 | Common:3; Rare:148 | ||||
| chr10:13099927-13100109 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:13161287-13161603 | Common:1; Rare:86 | ||||
| chr10:13299521-13299636 | Common:1; Rare:26 | ||||
| chr10:13300004-13300202 | Rare:69; Clinvar:2 | ||||
| chr10:13302010-13302230 | Common:2; Rare:48 | ||||
| chr10:13302316-13302525 | Rare:48 | ||||
| chr10:13346810-13347210 | Common:14; Rare:152 | ||||
| chr10:13348229-13348438 | Rare:57 | ||||
| chr10:13528027-13529345 | Common:20; Rare:637 | ||||
| chr10:13586778-13587008 | Common:3; Rare:74 | ||||
| chr10:13707300-13707900 | Common:3; Rare:146 | ||||
| chr10:14604387-14604544 | Common:2; Rare:78 | ||||
| chr10:14837912-14838334 | Common:2; Rare:127 | ||||
| chr10:14878084-14878484 | Common:1; Rare:175 |