| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39437078-39437464 | Common:4; Rare:138 | ||||
| chr2:43226598-43226862 | Common:2; Rare:103 | ||||
| chr2:43595967-43596169 | Common:1; Rare:64 | ||||
| chr2:46297142-46297413 | Common:5; Rare:105 | ||||
| chr2:46616974-46617223 | Common:6; Rare:92 | ||||
| chr2:46915723-46915935 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:53786852-53787307 | Common:1; Rare:178 | ||||
| chr2:53970991-53971122 | Common:4; Rare:51 | ||||
| chr2:55232351-55232759 | Common:3; Rare:124 | ||||
| chr2:61017159-61017264 | Common:2; Rare:28 | ||||
| chr2:61017406-61017747 | Common:1; Rare:99; Clinvar:1 | ||||
| chr2:61888385-61888706 | Common:1; Rare:145 | ||||
| chr2:63588731-63589020 | Rare:90 | ||||
| chr2:64019319-64019530 | Rare:72 | ||||
| chr2:64988336-64988501 | Common:1; Rare:30 |