| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61537992-61538143 | Common:2; Rare:28 | ||||
| chr2:61538204-61538436 | Common:1; Rare:52 | ||||
| chr2:61854016-61854223 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888373-61888727 | Common:1; Rare:157 | ||||
| chr2:61905762-61905847 | Rare:17 | ||||
| chr2:62706716-62706956 | Rare:44 | ||||
| chr2:63588727-63589040 | Rare:97 | ||||
| chr2:63840822-63841206 | Common:3; Rare:107 | ||||
| chr2:63841614-63841944 | Common:2; Rare:110 | ||||
| chr2:63842000-63842081 | Rare:12 | ||||
| chr2:64018941-64019083 | Rare:40 | ||||
| chr2:64019301-64019556 | Rare:83 | ||||
| chr2:64144357-64144709 | Common:4; Rare:98 | ||||
| chr2:64524103-64524370 | Common:3; Rare:76 | ||||
| chr2:64988346-64988516 | Common:1; Rare:32 |