| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39436639-39436746 | Rare:42 | ||||
| chr2:39437066-39437515 | Common:4; Rare:156 | ||||
| chr2:39778906-39779039 | Rare:37 | ||||
| chr2:39779098-39779401 | Common:4; Rare:101 | ||||
| chr2:42169132-42169508 | Common:1; Rare:170 | ||||
| chr2:42361069-42361260 | Rare:108 | ||||
| chr2:42361432-42361680 | Common:1; Rare:93 | ||||
| chr2:42568039-42568298 | Rare:74 | ||||
| chr2:42568821-42569027 | Common:1; Rare:54 | ||||
| chr2:42569131-42569438 | Common:2; Rare:70 | ||||
| chr2:42792223-42792361 | Rare:28 | ||||
| chr2:42792453-42792861 | Common:3; Rare:134 | ||||
| chr2:42793069-42793226 | Common:2; Rare:23 | ||||
| chr2:43595874-43596233 | Common:1; Rare:121 | ||||
| chr2:43995906-43996557 | Common:5; Rare:269; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 |