| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149546010-149546249 | Common:1; Rare:101 | ||||
| chr6:149648606-149648844 | Common:1; Rare:71 | ||||
| chr6:151452032-151452548 | Common:4; Rare:182 | ||||
| chr6:152982985-152983307 | Common:2; Rare:105 | ||||
| chr6:155314447-155314817 | Common:10; Rare:127 | ||||
| chr6:157323477-157323652 | Common:3; Rare:61 | ||||
| chr6:158168195-158168388 | Common:2; Rare:68 | ||||
| chr6:158644692-158644888 | Common:3; Rare:88 | ||||
| chr6:158649903-158650060 | Rare:35 | ||||
| chr6:159726948-159727162 | Rare:83 | ||||
| chr6:159789528-159789996 | Common:4; Rare:157 | ||||
| chr6:159790244-159790506 | Common:7; Rare:83 | ||||
| chr6:166342477-166342648 | Common:5; Rare:72 | ||||
| chr6:166999028-166999415 | Common:1; Rare:132 | ||||
| chr6:169751515-169751644 | Rare:48; Clinvar (benign):1 |