| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216606877-216607028 | Rare:30 | ||||
| chr2:216618890-216618972 | Common:1; Rare:14 | ||||
| chr2:216619171-216619263 | Rare:11 | ||||
| chr2:216619349-216620111 | Common:8; Rare:129 | ||||
| chr2:216633976-216634176 | Common:1; Rare:40 | ||||
| chr2:216635884-216636175 | Common:3; Rare:45 | ||||
| chr2:216636237-216636347 | Common:1; Rare:18 | ||||
| chr2:216636359-216636425 | Rare:6 | ||||
| chr2:216636668-216636912 | Rare:45 | ||||
| chr2:216636987-216637297 | Common:5; Rare:72 | ||||
| chr2:216691538-216691741 | Rare:34 | ||||
| chr2:216692925-216692981 | Rare:8 | ||||
| chr2:216693223-216693369 | Rare:23 | ||||
| chr2:216792326-216792431 | Common:2; Rare:22 | ||||
| chr2:217090064-217090175 | Rare:29 |