| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43621831-43622496 | Common:2; Rare:188; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43638681-43638947 | Rare:56 | ||||
| chr3:43690518-43691235 | Common:11; Rare:273; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:43691402-43691754 | Common:3; Rare:91 | ||||
| chr3:44338039-44338184 | Common:2; Rare:48 | ||||
| chr3:44338216-44338523 | Common:3; Rare:98 | ||||
| chr3:44338594-44338965 | Common:3; Rare:120 | ||||
| chr3:44477390-44477503 | Common:1; Rare:32 | ||||
| chr3:44477618-44477825 | Common:1; Rare:44 | ||||
| chr3:44510189-44510254 | Rare:14 | ||||
| chr3:44510573-44510841 | Common:6; Rare:77 | ||||
| chr3:44511055-44511144 | Rare:18 | ||||
| chr3:44555071-44555470 | Common:1; Rare:102 | ||||
| chr3:44584695-44584992 | Rare:55 | ||||
| chr3:44624817-44625132 | Common:3; Rare:81 |