| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169668082-169668392 | Common:1; Rare:68 | ||||
| chr3:169764751-169764825 | Rare:13; Clinvar:3 | ||||
| chr3:169764833-169764890 | Rare:19; Clinvar:7; Clinvar (pathogenic):1 | ||||
| chr3:169764892-169765203 | Common:1; Rare:118; Clinvar:12; Clinvar (pathogenic):5 | ||||
| chr3:170083282-170083363 | Rare:12 | ||||
| chr3:170132784-170133050 | Rare:32 | ||||
| chr3:171110756-171111004 | Rare:52 | ||||
| chr3:172069794-172069924 | Rare:25 | ||||
| chr3:172070363-172070436 | Common:1; Rare:8 | ||||
| chr3:172202700-172202948 | Common:2; Rare:38 | ||||
| chr3:179171158-179171198 | Rare:11 | ||||
| chr3:179180152-179180391 | Rare:34 | ||||
| chr3:179189869-179189994 | Rare:23 | ||||
| chr3:179220717-179221011 | Common:3; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:179229872-179230286 | Common:1; Rare:61; Clinvar (benign):1 |