| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:46882154-46882478 | Common:1; Rare:97 | ||||
| chr3:46979494-46979864 | Common:3; Rare:96; Clinvar:2 | ||||
| chr3:46981943-46982185 | Rare:38 | ||||
| chr3:47002144-47002520 | Rare:130; Clinvar:2 | ||||
| chr3:47003568-47003879 | Common:2; Rare:55; Clinvar:1 | ||||
| chr3:47163878-47164281 | Common:1; Rare:113; Clinvar (pathogenic):1 | ||||
| chr3:47380573-47381174 | Common:1; Rare:179 | ||||
| chr3:47381427-47381524 | Rare:26 | ||||
| chr3:47405657-47406046 | Common:2; Rare:123 | ||||
| chr3:47409484-47409834 | Rare:105 | ||||
| chr3:47427240-47427470 | Rare:60 | ||||
| chr3:47475788-47476068 | Common:3; Rare:110 | ||||
| chr3:47513345-47513496 | Common:1; Rare:36 | ||||
| chr3:47513672-47513788 | Rare:34 | ||||
| chr3:47781682-47782073 | Common:1; Rare:153 |