| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792414-9792552 | Rare:37 | ||||
| chr3:9792732-9793115 | Common:3; Rare:131 | ||||
| chr3:9843975-9844135 | Common:2; Rare:63 | ||||
| chr3:9933523-9933857 | Common:2; Rare:135; Clinvar:3 | ||||
| chr3:10026341-10026459 | Rare:33 | ||||
| chr3:10141728-10141808 | Common:1; Rare:26; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:11225908-11225983 | Rare:10 | ||||
| chr3:12664084-12664300 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124746-14125100 | Common:4; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178555-14178861 | Common:2; Rare:159; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14947412-14947546 | Common:2; Rare:63 | ||||
| chr3:15427510-15427629 | Rare:37 | ||||
| chr3:15601498-15601798 | Common:4; Rare:123; Clinvar:1 | ||||
| chr3:16264881-16265201 | Common:2; Rare:104 | ||||
| chr3:19947071-19947399 | Common:4; Rare:123 |