| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:135344-135557 | Rare:54 | ||||
| chr10:988335-988492 | Common:1; Rare:64 | ||||
| chr10:1048865-1049086 | Common:2; Rare:117 | ||||
| chr10:3785149-3785551 | Common:4; Rare:149 | ||||
| chr10:6202732-6202932 | Common:4; Rare:53 | ||||
| chr10:6580237-6580580 | Common:11; Rare:110 | ||||
| chr10:7787958-7788263 | Common:1; Rare:123 | ||||
| chr10:12068788-12069014 | Common:2; Rare:85 | ||||
| chr10:12195838-12196241 | Rare:107 | ||||
| chr10:13099929-13100241 | Common:3; Rare:76; Clinvar:3; Clinvar (benign):5 | ||||
| chr10:14837978-14838352 | Common:2; Rare:104 | ||||
| chr10:14878637-14878901 | Common:2; Rare:79 | ||||
| chr10:15097306-15097378 | Common:1; Rare:33 | ||||
| chr10:15860453-15860589 | Rare:37 | ||||
| chr10:17228418-17228675 | Common:2; Rare:68 |