| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:168834081-168834313 | Common:3; Rare:43 | ||||
| chr2:168851048-168851366 | Common:1; Rare:86 | ||||
| chr2:169828022-169828059 | Common:1; Rare:6 | ||||
| chr2:170751686-170751709 | Rare:4 | ||||
| chr2:170770746-170771108 | Common:2; Rare:64 | ||||
| chr2:171743758-171744189 | Common:3; Rare:88 | ||||
| chr2:172429786-172429895 | Rare:15 | ||||
| chr2:172431556-172431647 | Rare:9 | ||||
| chr2:172478421-172478659 | Common:2; Rare:47 | ||||
| chr2:172484614-172484942 | Rare:60 | ||||
| chr2:172487001-172487460 | Common:3; Rare:124; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:172489199-172489607 | Common:1; Rare:89 | ||||
| chr2:172503874-172504051 | Rare:30 | ||||
| chr2:172995579-172995796 | Common:1; Rare:31 | ||||
| chr2:174486253-174486283 | Rare:7 |