| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215311910-215312089 | Common:5; Rare:71 | ||||
| chr2:215435962-215436241 | Common:2; Rare:88 | ||||
| chr2:216081756-216081906 | Common:1; Rare:50 | ||||
| chr2:216498740-216498886 | Common:5; Rare:60 | ||||
| chr2:216694692-216694803 | Rare:33 | ||||
| chr2:217978622-217978713 | Rare:25 | ||||
| chr2:217978839-217978976 | Common:1; Rare:40 | ||||
| chr2:218217049-218217226 | Common:1; Rare:65 | ||||
| chr2:218270075-218270538 | Common:5; Rare:146; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218322982-218323307 | Common:6; Rare:107 | ||||
| chr2:218568303-218568640 | Common:3; Rare:90 | ||||
| chr2:218659474-218659738 | Common:2; Rare:63 | ||||
| chr2:218671977-218672086 | Rare:37 | ||||
| chr2:219176926-219177073 | Common:4; Rare:45 | ||||
| chr2:219206681-219206916 | Rare:86 |