| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43690530-43690598 | Common:1; Rare:16 | ||||
| chr3:43690726-43691166 | Common:9; Rare:211; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:43691385-43691441 | Common:1; Rare:18 | ||||
| chr3:43691480-43691754 | Common:2; Rare:69 | ||||
| chr3:44338047-44338218 | Common:2; Rare:54 | ||||
| chr3:44338237-44338508 | Common:3; Rare:86 | ||||
| chr3:44338641-44338964 | Common:3; Rare:110 | ||||
| chr3:44338997-44339130 | Common:1; Rare:23 | ||||
| chr3:44477390-44477480 | Common:1; Rare:26 | ||||
| chr3:44477620-44477821 | Common:1; Rare:42 | ||||
| chr3:44510571-44510837 | Common:6; Rare:76 | ||||
| chr3:44511068-44511293 | Rare:50 | ||||
| chr3:44555079-44555477 | Common:1; Rare:101 | ||||
| chr3:44624745-44624802 | Rare:9 | ||||
| chr3:44624817-44625109 | Common:2; Rare:76 |