| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017200-61017309 | Common:2; Rare:25 | ||||
| chr2:61017429-61017767 | Common:1; Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61144901-61145165 | Common:3; Rare:90 | ||||
| chr2:61470667-61470983 | Rare:107 | ||||
| chr2:61471085-61471350 | Common:1; Rare:98 | ||||
| chr2:61854033-61854228 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888448-61888693 | Common:1; Rare:111 | ||||
| chr2:63588926-63589025 | Rare:37 | ||||
| chr2:63840844-63841160 | Common:2; Rare:85 | ||||
| chr2:63841593-63841896 | Common:2; Rare:102 | ||||
| chr2:65056160-65056473 | Common:2; Rare:109 | ||||
| chr2:65227591-65227905 | Rare:91 | ||||
| chr2:66434874-66435171 | Common:1; Rare:68 | ||||
| chr2:68157472-68157955 | Common:2; Rare:248 | ||||
| chr2:68467292-68467594 | Common:1; Rare:72 |