| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:41238969-41239359 | Common:1; Rare:127; Clinvar (benign):2 | ||||
| chr3:41962007-41962562 | Common:9; Rare:137 | ||||
| chr3:42013536-42013753 | Common:5; Rare:67 | ||||
| chr3:42160071-42160228 | Common:1; Rare:33 | ||||
| chr3:42581881-42582143 | Common:3; Rare:80 | ||||
| chr3:42582255-42582453 | Common:1; Rare:48 | ||||
| chr3:42600355-42600778 | Common:3; Rare:164 | ||||
| chr3:42600870-42601010 | Rare:52 | ||||
| chr3:42630848-42631316 | Common:1; Rare:84 | ||||
| chr3:42653541-42653712 | Rare:36 | ||||
| chr3:42654129-42654176 | Common:1; Rare:9 | ||||
| chr3:42685233-42685542 | Rare:55 | ||||
| chr3:42701518-42701673 | Common:1; Rare:23 | ||||
| chr3:42702636-42702907 | Rare:64 | ||||
| chr3:42773206-42773360 | Common:1; Rare:45 |