| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207625863-207626263 | Common:8; Rare:182 | ||||
| chr2:207711280-207711742 | Common:3; Rare:334 | ||||
| chr2:207711955-207712560 | Common:3; Rare:260 | ||||
| chr2:207769440-207769835 | Common:4; Rare:123 | ||||
| chr2:207769802-207770257 | Common:3; Rare:338 | ||||
| chr2:208025433-208025691 | Common:5; Rare:130 | ||||
| chr2:208254164-208254564 | Common:2; Rare:158 | ||||
| chr2:208254974-208255368 | Common:6; Rare:252 | ||||
| chr2:208265999-208266410 | Common:24; Rare:328; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:209423700-209424222 | Common:7; Rare:343 | ||||
| chr2:210002399-210002818 | Common:18; Rare:342 | ||||
| chr2:210002854-210003630 | Common:3; Rare:241 | ||||
| chr2:210170619-210170987 | Common:6; Rare:359 | ||||
| chr2:210171234-210171630 | Common:12; Rare:382 | ||||
| chr2:210224940-210225260 | Common:1; Rare:82; Clinvar:2 |