| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:13420177-13420470 | Common:1; Rare:91 | ||||
| chr3:13480036-13480339 | Common:2; Rare:71 | ||||
| chr3:14124728-14125173 | Common:4; Rare:126; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178881 | Common:2; Rare:169; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402326-14402653 | Common:1; Rare:89 | ||||
| chr3:14540324-14540465 | Common:2; Rare:50 | ||||
| chr3:14651468-14651839 | Rare:116 | ||||
| chr3:14947277-14947559 | Common:3; Rare:127 | ||||
| chr3:14948024-14948271 | Rare:103 | ||||
| chr3:14948407-14948735 | Common:2; Rare:110 | ||||
| chr3:15065081-15065399 | Common:2; Rare:113 | ||||
| chr3:15099095-15099291 | Rare:50 | ||||
| chr3:15206047-15206278 | Rare:88 | ||||
| chr3:15427459-15427775 | Common:2; Rare:108 | ||||
| chr3:15601469-15602082 | Common:6; Rare:274; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 |