| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201119009-201119317 | Rare:53 | ||||
| chr2:201122390-201122457 | Rare:17 | ||||
| chr2:201122516-201122823 | Rare:48 | ||||
| chr2:201129220-201129358 | Rare:36 | ||||
| chr2:201257979-201258135 | Common:1; Rare:25 | ||||
| chr2:201258169-201258348 | Common:2; Rare:55; Clinvar (benign):2 | ||||
| chr2:201260420-201260626 | Rare:44 | ||||
| chr2:201451435-201451856 | Common:2; Rare:105 | ||||
| chr2:201642643-201642754 | Rare:57 | ||||
| chr2:201643443-201643799 | Common:2; Rare:70; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:202238445-202238625 | Rare:63; Clinvar:1 | ||||
| chr2:202265546-202265842 | Common:1; Rare:96 | ||||
| chr2:202376074-202376527 | Rare:157 | ||||
| chr2:202377023-202377372 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:202634795-202635032 | Common:5; Rare:87 |