| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48918787-48918895 | Common:2; Rare:62 | ||||
| chr3:49104729-49104891 | Rare:66; Clinvar (benign):3 | ||||
| chr3:49340020-49340102 | Common:1; Rare:41 | ||||
| chr3:49411883-49412438 | Common:2; Rare:204 | ||||
| chr3:49689461-49689573 | Rare:29 | ||||
| chr3:49786528-49786781 | Rare:77 | ||||
| chr3:50350718-50350894 | Common:1; Rare:25 | ||||
| chr3:51385025-51385356 | Common:2; Rare:102 | ||||
| chr3:51983337-51983537 | Rare:44 | ||||
| chr3:52239075-52239273 | Common:2; Rare:69 | ||||
| chr3:52455425-52455644 | Common:2; Rare:73 | ||||
| chr3:52685944-52686049 | Common:1; Rare:36 | ||||
| chr3:52705558-52706213 | Common:4; Rare:208 | ||||
| chr3:53347525-53347754 | Common:1; Rare:70 | ||||
| chr3:53891794-53892027 | Common:2; Rare:71 |