| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104720-49104910 | Rare:82; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49120754-49120997 | Rare:74 | ||||
| chr3:49166294-49166438 | Common:1; Rare:35 | ||||
| chr3:49340027-49340189 | Common:2; Rare:58 | ||||
| chr3:49358281-49358497 | Common:2; Rare:115 | ||||
| chr3:49411918-49412213 | Common:1; Rare:106 | ||||
| chr3:49429244-49429462 | Common:1; Rare:49 | ||||
| chr3:49689460-49689605 | Rare:45 | ||||
| chr3:49786522-49786781 | Rare:78 | ||||
| chr3:49856529-49856704 | Common:2; Rare:48 | ||||
| chr3:50088788-50088980 | Rare:50 | ||||
| chr3:50292401-50292680 | Rare:113 | ||||
| chr3:50299282-50299583 | Rare:69 | ||||
| chr3:50350718-50350892 | Common:1; Rare:25 | ||||
| chr3:50616924-50617174 | Common:7; Rare:50 |