| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169765056-169765185 | Rare:59; Clinvar (pathogenic):2 | ||||
| chr3:170355761-170356161 | Common:2; Rare:149 | ||||
| chr3:170356268-170356696 | Common:6; Rare:210 | ||||
| chr3:170425570-170426210 | Common:5; Rare:94 | ||||
| chr3:170470628-170471028 | Rare:112 | ||||
| chr3:171159190-171159530 | Common:9; Rare:61 | ||||
| chr3:171173903-171174105 | Common:2; Rare:42 | ||||
| chr3:171306759-171306983 | Rare:71 | ||||
| chr3:171383244-171383779 | Common:5; Rare:131 | ||||
| chr3:171383761-171384161 | Common:2; Rare:90 | ||||
| chr3:171457371-171458401 | Common:6; Rare:326 | ||||
| chr3:171458778-171459385 | Common:4; Rare:130 | ||||
| chr3:171466885-171467035 | Rare:43 | ||||
| chr3:171975262-171975433 | Rare:32 | ||||
| chr3:172041524-172041924 | Common:1; Rare:71 |