| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69013142-69013235 | Common:4; Rare:24 | ||||
| chr2:69013242-69013466 | Common:1; Rare:48 | ||||
| chr2:69013550-69013854 | Common:2; Rare:76 | ||||
| chr2:69013871-69013914 | Rare:9 | ||||
| chr2:69386956-69386983 | Rare:2 | ||||
| chr2:69386986-69387074 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr2:69387137-69387530 | Common:1; Rare:112; Clinvar:2 | ||||
| chr2:69436922-69437028 | Common:1; Rare:23 | ||||
| chr2:69437067-69437226 | Rare:47 | ||||
| chr2:69437286-69437720 | Common:2; Rare:200; Clinvar:7; Clinvar (benign):6 | ||||
| chr2:69643187-69643465 | Rare:61 | ||||
| chr2:69643608-69644286 | Common:7; Rare:171 | ||||
| chr2:69644423-69644466 | Rare:6 | ||||
| chr2:69741358-69741490 | Rare:30 | ||||
| chr2:69741672-69741863 | Common:3; Rare:34 |