| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:1048872-1049073 | Common:2; Rare:110 | ||||
| chr10:1049111-1049132 | Common:1; Rare:4 | ||||
| chr10:3785251-3785554 | Common:4; Rare:105 | ||||
| chr10:7787958-7788232 | Common:1; Rare:113 | ||||
| chr10:12043168-12043365 | Common:2; Rare:59 | ||||
| chr10:12068758-12068987 | Common:2; Rare:80 | ||||
| chr10:12195800-12196251 | Rare:124 | ||||
| chr10:13099945-13100234 | Common:3; Rare:74; Clinvar:3; Clinvar (benign):5 | ||||
| chr10:13348005-13348262 | Rare:87 | ||||
| chr10:14838034-14838345 | Common:2; Rare:81 | ||||
| chr10:14878645-14878891 | Common:2; Rare:73 | ||||
| chr10:14954023-14954195 | Rare:61 | ||||
| chr10:15860494-15860592 | Rare:24 | ||||
| chr10:17228464-17228675 | Common:1; Rare:57 | ||||
| chr10:17643898-17644269 | Common:2; Rare:110 |