| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38751350-38751592 | Common:3; Rare:103 | ||||
| chr2:38875886-38876066 | Common:1; Rare:67 | ||||
| chr2:39121022-39121093 | Rare:18 | ||||
| chr2:39437115-39437464 | Common:4; Rare:123 | ||||
| chr2:40451994-40452256 | Common:4; Rare:97 | ||||
| chr2:42169162-42169431 | Common:1; Rare:134 | ||||
| chr2:42792543-42792849 | Common:3; Rare:89 | ||||
| chr2:43595953-43596205 | Common:1; Rare:91 | ||||
| chr2:44361479-44362007 | Common:3; Rare:165 | ||||
| chr2:46297249-46297409 | Common:3; Rare:59 | ||||
| chr2:46543117-46543176 | Rare:13 | ||||
| chr2:46616984-46617273 | Common:7; Rare:127 | ||||
| chr2:46915733-46916180 | Common:4; Rare:147; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176439-47176759 | Common:4; Rare:157; Clinvar (benign):5 | ||||
| chr2:47344968-47345196 | Common:1; Rare:64 |