| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203706590-203706730 | Rare:31 | ||||
| chr2:205682341-205682559 | Rare:38 | ||||
| chr2:206085567-206086357 | Common:5; Rare:173 | ||||
| chr2:206159356-206159683 | Common:3; Rare:102; Clinvar (benign):1 | ||||
| chr2:206159801-206159997 | Common:1; Rare:67 | ||||
| chr2:206160061-206160226 | Common:1; Rare:60 | ||||
| chr2:206274561-206274742 | Common:1; Rare:54 | ||||
| chr2:206274816-206275094 | Common:1; Rare:83 | ||||
| chr2:206765184-206765693 | Common:4; Rare:143; Clinvar:5; Clinvar (benign):6 | ||||
| chr2:206765804-206765915 | Rare:31 | ||||
| chr2:207164740-207165113 | Common:3; Rare:79 | ||||
| chr2:207165158-207165287 | Rare:30 | ||||
| chr2:207165871-207165974 | Rare:24 | ||||
| chr2:207165977-207166452 | Common:4; Rare:165 | ||||
| chr2:207166732-207167027 | Common:4; Rare:107 |