| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14124191-14124593 | Common:7; Rare:207 | ||||
| chr3:14124698-14125174 | Common:8; Rare:277; Clinvar:8; Clinvar (benign):2 | ||||
| chr3:14178540-14178862 | Common:4; Rare:317; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402281-14402798 | Common:9; Rare:231 | ||||
| chr3:14651432-14651867 | Common:2; Rare:236 | ||||
| chr3:14947355-14947628 | Common:5; Rare:217 | ||||
| chr3:14948319-14948674 | Common:4; Rare:209 | ||||
| chr3:15065204-15065403 | Common:4; Rare:147 | ||||
| chr3:15099095-15099303 | Rare:95 | ||||
| chr3:15205976-15206343 | Common:2; Rare:237 | ||||
| chr3:15427465-15427659 | Common:2; Rare:137 | ||||
| chr3:15601501-15601818 | Common:9; Rare:263; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:15601813-15602050 | Common:3; Rare:229; Clinvar:10; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr3:15858940-15859086 | Rare:32 | ||||
| chr3:15859447-15859680 | Common:11; Rare:96 |