| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:55216309-55216679 | Common:3; Rare:62 | ||||
| chr19:55668537-55668735 | Common:1; Rare:48 | ||||
| chr19:56765240-56765377 | Common:1; Rare:41 | ||||
| chr2:739926-740204 | Common:27; Rare:75 | ||||
| chr2:740255-740469 | Common:18; Rare:43 | ||||
| chr2:2333188-2333356 | Rare:48 | ||||
| chr2:5691251-5691473 | Rare:64 | ||||
| chr2:5693582-5693876 | Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:5697409-5697755 | Common:1; Rare:80 | ||||
| chr2:5700132-5700237 | Rare:19 | ||||
| chr2:5981593-5981802 | Rare:33 | ||||
| chr2:5981853-5981999 | Rare:31 | ||||
| chr2:5982252-5982599 | Common:2; Rare:70 | ||||
| chr2:10441580-10441829 | Common:1; Rare:77 | ||||
| chr2:15941227-15941378 | Common:1; Rare:34 |