| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31753802-31754122 | Common:1; Rare:113 | ||||
| chr22:31944301-31944768 | Common:7; Rare:178 | ||||
| chr22:32474660-32475059 | Common:4; Rare:131; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:32475129-32475341 | Common:2; Rare:70; Clinvar (benign):1 | ||||
| chr22:32801841-32802138 | Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:35257397-35257556 | Common:1; Rare:52 | ||||
| chr22:35399905-35400197 | Rare:102 | ||||
| chr22:35648264-35648559 | Common:2; Rare:50 | ||||
| chr22:36160703-36161028 | Common:4; Rare:105 | ||||
| chr22:36239445-36239671 | Rare:80 | ||||
| chr22:36285864-36286185 | Rare:73; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:36328682-36328895 | Rare:51 | ||||
| chr22:36387935-36388322 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481535-36481737 | Common:2; Rare:61 | ||||
| chr22:36507024-36507147 | Common:2; Rare:41 |