| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17453746-17454282 | Common:11; Rare:163 | ||||
| chr10:17454479-17454915 | Common:4; Rare:198 | ||||
| chr10:17616680-17617100 | Common:6; Rare:213 | ||||
| chr10:17617218-17617674 | Common:16; Rare:318 | ||||
| chr10:17643819-17644306 | Common:6; Rare:425 | ||||
| chr10:18140317-18140443 | Common:1; Rare:34 | ||||
| chr10:18400424-18400725 | Common:2; Rare:62 | ||||
| chr10:18651524-18651844 | Common:3; Rare:218 | ||||
| chr10:18659148-18659609 | Common:6; Rare:354 | ||||
| chr10:19203168-19204135 | Common:19; Rare:390 | ||||
| chr10:19815073-19815931 | Common:4; Rare:269 | ||||
| chr10:19816030-19816662 | Common:21; Rare:361 | ||||
| chr10:21172823-21174702 | Common:24; Rare:907; Clinvar (benign):6 | ||||
| chr10:21496500-21497101 | Common:3; Rare:297 | ||||
| chr10:21497211-21497438 | Common:5; Rare:94 |