| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017420-61017750 | Common:1; Rare:98; Clinvar:2 | ||||
| chr2:61144920-61145165 | Common:3; Rare:82 | ||||
| chr2:61470675-61470987 | Rare:104 | ||||
| chr2:61536710-61536767 | Rare:18 | ||||
| chr2:61538503-61538824 | Common:1; Rare:81 | ||||
| chr2:61854010-61854079 | Common:1; Rare:31; Clinvar:1 | ||||
| chr2:61888450-61888731 | Common:1; Rare:122 | ||||
| chr2:61905567-61905697 | Rare:53 | ||||
| chr2:63588218-63589025 | Common:2; Rare:251; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:63840817-63841178 | Common:2; Rare:99 | ||||
| chr2:63841673-63841934 | Common:1; Rare:94 | ||||
| chr2:64144254-64144683 | Common:4; Rare:121 | ||||
| chr2:64524113-64524408 | Common:3; Rare:87 | ||||
| chr2:64653768-64654067 | Common:1; Rare:102 | ||||
| chr2:65056160-65056461 | Common:2; Rare:103 |