| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190469400-190469527 | Rare:19 | ||||
| chr2:190534655-190534846 | Common:1; Rare:62 | ||||
| chr2:190649449-190649609 | Common:1; Rare:48 | ||||
| chr2:191014080-191014431 | Common:3; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191021007-191021130 | Common:1; Rare:21 | ||||
| chr2:191245219-191245560 | Common:3; Rare:113 | ||||
| chr2:191246154-191246305 | Common:1; Rare:44 | ||||
| chr2:191677823-191678201 | Common:4; Rare:107 | ||||
| chr2:191678565-191678597 | Rare:15 | ||||
| chr2:191678601-191678668 | Rare:25 | ||||
| chr2:191678842-191679127 | Rare:80 | ||||
| chr2:191846722-191847093 | Rare:106 | ||||
| chr2:191847102-191847425 | Rare:52 | ||||
| chr2:195656823-195657321 | Common:2; Rare:149 | ||||
| chr2:196068808-196068919 | Common:1; Rare:27 |