| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73283764-73284062 | Common:1; Rare:58 | ||||
| chr2:73284388-73284548 | Rare:43 | ||||
| chr2:73293527-73293858 | Common:1; Rare:137 | ||||
| chr2:73385569-73386124 | Common:4; Rare:249; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr2:73386129-73386390 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:73737200-73737627 | Common:3; Rare:139 | ||||
| chr2:73780006-73780282 | Common:2; Rare:109 | ||||
| chr2:73828783-73829150 | Common:2; Rare:86 | ||||
| chr2:73926681-73926971 | Common:2; Rare:138; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:73927081-73927149 | Rare:15 | ||||
| chr2:73927184-73927475 | Rare:63 | ||||
| chr2:74147601-74147740 | Rare:23 | ||||
| chr2:74147793-74148331 | Common:4; Rare:130; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:74148346-74148458 | Common:1; Rare:28 | ||||
| chr2:74178365-74178486 | Rare:31 |