| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:46693598-46693794 | Common:2; Rare:42 | ||||
| chr3:46976732-46977082 | Common:2; Rare:73 | ||||
| chr3:46979474-46979882 | Common:3; Rare:105; Clinvar:2 | ||||
| chr3:46981980-46982186 | Rare:33 | ||||
| chr3:46982197-46982635 | Common:4; Rare:65 | ||||
| chr3:46995733-46996022 | Rare:88; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr3:47001735-47002520 | Common:4; Rare:272; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:47005068-47005533 | Common:1; Rare:128; Clinvar (benign):1 | ||||
| chr3:47163915-47164232 | Common:1; Rare:88 | ||||
| chr3:47380812-47381144 | Rare:107 | ||||
| chr3:47381427-47381750 | Rare:74 | ||||
| chr3:47409284-47409509 | Rare:53 | ||||
| chr3:47420831-47420894 | Rare:12 | ||||
| chr3:47475801-47476058 | Common:3; Rare:105 | ||||
| chr3:47513633-47513767 | Common:1; Rare:46 |