| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:144404571-144404928 | Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:148020678-148021011 | Common:2; Rare:72 | ||||
| chr2:149330405-149330664 | Common:2; Rare:101 | ||||
| chr2:149587306-149587347 | Rare:8 | ||||
| chr2:149587681-149587905 | Common:1; Rare:67; Clinvar:1 | ||||
| chr2:151828355-151828610 | Common:3; Rare:75 | ||||
| chr2:152175719-152176086 | Common:2; Rare:98 | ||||
| chr2:152717829-152717969 | Rare:60 | ||||
| chr2:152717991-152718305 | Common:1; Rare:103 | ||||
| chr2:152718490-152718662 | Rare:69 | ||||
| chr2:158968475-158968678 | Rare:62 | ||||
| chr2:159615216-159615343 | Common:2; Rare:29 | ||||
| chr2:159616422-159616624 | Common:2; Rare:42 | ||||
| chr2:159712417-159712584 | Common:2; Rare:67 | ||||
| chr2:161160228-161160469 | Common:2; Rare:67 |