| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42792221-42792246 | Common:1; Rare:2 | ||||
| chr2:42792251-42792366 | Rare:27 | ||||
| chr2:42792449-42792784 | Common:2; Rare:110 | ||||
| chr2:42793062-42793226 | Common:2; Rare:24 | ||||
| chr2:43225886-43226064 | Common:1; Rare:63 | ||||
| chr2:43226178-43226455 | Common:1; Rare:115 | ||||
| chr2:43226541-43226926 | Common:4; Rare:154 | ||||
| chr2:43595870-43596324 | Common:2; Rare:153 | ||||
| chr2:43995923-43996491 | Common:5; Rare:252; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:44167762-44168150 | Common:4; Rare:152 | ||||
| chr2:44168534-44168958 | Common:1; Rare:136 | ||||
| chr2:44361447-44361563 | Common:1; Rare:46 | ||||
| chr2:44361777-44362129 | Common:2; Rare:118 | ||||
| chr2:45610814-45610872 | Rare:26 | ||||
| chr2:45611157-45611407 | Rare:89 |