| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216012968-216013930 | Common:14; Rare:378 | ||||
| chr2:216081714-216081979 | Common:3; Rare:209 | ||||
| chr2:216107741-216108603 | Common:8; Rare:223 | ||||
| chr2:216108852-216109607 | Common:35; Rare:501 | ||||
| chr2:216412439-216412804 | Common:5; Rare:120; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:216498649-216498982 | Common:25; Rare:330 | ||||
| chr2:216633223-216633562 | Common:6; Rare:301 | ||||
| chr2:216633589-216633855 | Common:3; Rare:116 | ||||
| chr2:217434184-217434418 | Rare:82 | ||||
| chr2:217944021-217944218 | Common:2; Rare:67 | ||||
| chr2:217978750-217979167 | Common:5; Rare:164 | ||||
| chr2:218216848-218217303 | Common:7; Rare:314 | ||||
| chr2:218217620-218218130 | Common:1; Rare:105 | ||||
| chr2:218245360-218245610 | Rare:61 | ||||
| chr2:218270037-218270618 | Common:15; Rare:499; Clinvar:15; Clinvar (benign):5 |