| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:988294-988482 | Common:1; Rare:75 | ||||
| chr10:1048874-1049086 | Common:2; Rare:112 | ||||
| chr10:3785251-3785554 | Common:4; Rare:105 | ||||
| chr10:6580237-6580458 | Common:10; Rare:74 | ||||
| chr10:7787940-7788240 | Common:1; Rare:126 | ||||
| chr10:12043171-12043381 | Common:2; Rare:62 | ||||
| chr10:12195815-12196248 | Rare:119 | ||||
| chr10:13099976-13100251 | Common:3; Rare:67; Clinvar:3; Clinvar (benign):5 | ||||
| chr10:14838002-14838352 | Common:2; Rare:91 | ||||
| chr10:14878627-14878916 | Common:2; Rare:89 | ||||
| chr10:14954023-14954160 | Rare:44 | ||||
| chr10:15860494-15860583 | Rare:23 | ||||
| chr10:16817351-16817757 | Common:4; Rare:147 | ||||
| chr10:17228489-17228675 | Common:1; Rare:54 | ||||
| chr10:17230545-17230710 | Rare:70; Clinvar:1 |