| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13099987-13100302 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13300035-13300149 | Rare:46; Clinvar:1 | ||||
| chr10:13348003-13348363 | Rare:121 | ||||
| chr10:13707573-13707772 | Common:1; Rare:45 | ||||
| chr10:14837974-14838380 | Common:2; Rare:118 | ||||
| chr10:14878637-14878891 | Common:2; Rare:76 | ||||
| chr10:14954023-14954201 | Rare:65 | ||||
| chr10:15097301-15097403 | Common:1; Rare:50 | ||||
| chr10:15860342-15860589 | Common:1; Rare:61 | ||||
| chr10:16817499-16817842 | Common:1; Rare:98 | ||||
| chr10:17228364-17228606 | Common:3; Rare:57 | ||||
| chr10:17228613-17228675 | Common:1; Rare:20 | ||||
| chr10:17228990-17229026 | Common:1; Rare:7 | ||||
| chr10:17230526-17230710 | Rare:79; Clinvar:1 | ||||
| chr10:17643898-17644315 | Common:2; Rare:128 |