| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:25016421-25016749 | Common:10; Rare:132 | ||||
| chr10:25016873-25017375 | Common:6; Rare:174 | ||||
| chr10:26697139-26697450 | Common:3; Rare:68 | ||||
| chr10:26697509-26698010 | Common:4; Rare:147; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:26860767-26861424 | Common:8; Rare:173 | ||||
| chr10:27100138-27100269 | Common:1; Rare:73; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:27100352-27100688 | Common:5; Rare:87; Clinvar:4; Clinvar (benign):3 | ||||
| chr10:27153891-27153982 | Common:2; Rare:21 | ||||
| chr10:27153987-27154133 | Common:1; Rare:35 | ||||
| chr10:27154296-27154559 | Rare:73 | ||||
| chr10:27154947-27155038 | Rare:15 | ||||
| chr10:27155048-27155501 | Common:7; Rare:166; Clinvar:7; Clinvar (benign):8 | ||||
| chr10:27155730-27155771 | Common:1; Rare:7 | ||||
| chr10:27155785-27156190 | Common:7; Rare:86 | ||||
| chr10:27240292-27240703 | Common:2; Rare:121 |