| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49022026-49022145 | Rare:40 | ||||
| chr3:49104692-49104910 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:49132953-49133148 | Rare:39; Clinvar:2 | ||||
| chr3:49166287-49166443 | Common:1; Rare:40 | ||||
| chr3:49171424-49171633 | Common:3; Rare:45 | ||||
| chr3:49340026-49340110 | Common:2; Rare:38 | ||||
| chr3:49358285-49358486 | Common:2; Rare:108 | ||||
| chr3:49411898-49412213 | Common:1; Rare:110 | ||||
| chr3:49429269-49429359 | Rare:23 | ||||
| chr3:49470004-49470319 | Common:1; Rare:94 | ||||
| chr3:49674228-49674395 | Common:1; Rare:62 | ||||
| chr3:49689460-49689606 | Rare:46 | ||||
| chr3:49723922-49724221 | Common:9; Rare:104 | ||||
| chr3:49856521-49856727 | Common:2; Rare:60 | ||||
| chr3:50292375-50292637 | Common:1; Rare:104 |