| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32010388-32010503 | Rare:40 | ||||
| chr2:32010740-32011172 | Common:1; Rare:125 | ||||
| chr2:32039728-32040034 | Common:2; Rare:86 | ||||
| chr2:32040086-32040174 | Rare:19 | ||||
| chr2:32063097-32063157 | Rare:18 | ||||
| chr2:32063273-32063879 | Common:2; Rare:213; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:32063888-32064101 | Common:1; Rare:103; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:32064178-32064239 | Rare:11 | ||||
| chr2:32165516-32166017 | Common:3; Rare:177 | ||||
| chr2:32277719-32277987 | Common:1; Rare:63 | ||||
| chr2:32278137-32278242 | Rare:37 | ||||
| chr2:32278343-32278405 | Rare:12 | ||||
| chr2:32356875-32357378 | Common:5; Rare:205 | ||||
| chr2:32627619-32627662 | Rare:9 | ||||
| chr2:32627896-32628180 | Rare:83 |