| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61144921-61145165 | Common:3; Rare:82 | ||||
| chr2:61177279-61177472 | Common:3; Rare:83 | ||||
| chr2:61471245-61471387 | Common:2; Rare:52 | ||||
| chr2:61536745-61536794 | Rare:11 | ||||
| chr2:61537033-61537140 | Rare:21 | ||||
| chr2:61854019-61854208 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888470-61888727 | Common:1; Rare:110 | ||||
| chr2:63588236-63588540 | Common:1; Rare:92; Clinvar:6 | ||||
| chr2:63588734-63589045 | Rare:98 | ||||
| chr2:63840822-63841197 | Common:3; Rare:103 | ||||
| chr2:63841673-63841963 | Common:1; Rare:101 | ||||
| chr2:64524123-64524469 | Common:1; Rare:114 | ||||
| chr2:64653738-64654071 | Common:1; Rare:113 | ||||
| chr2:64989101-64989399 | Common:6; Rare:82 | ||||
| chr2:65056160-65056473 | Common:2; Rare:109 |