| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16884828-16885228 | Common:8; Rare:98 | ||||
| chr3:17742650-17742952 | Common:3; Rare:106 | ||||
| chr3:19946974-19947415 | Common:5; Rare:166 | ||||
| chr3:23202926-23203200 | Common:1; Rare:98 | ||||
| chr3:23916870-23917204 | Rare:132 | ||||
| chr3:25428103-25428398 | Rare:67 | ||||
| chr3:25783377-25783640 | Common:2; Rare:85; Clinvar (benign):3 | ||||
| chr3:25789966-25790126 | Common:5; Rare:63 | ||||
| chr3:28348779-28349188 | Common:4; Rare:128 | ||||
| chr3:29280837-29280890 | Common:1; Rare:14 | ||||
| chr3:29280997-29281393 | Common:13; Rare:73 | ||||
| chr3:30606292-30606530 | Common:1; Rare:58; Clinvar:1 | ||||
| chr3:31532383-31532641 | Common:2; Rare:70 | ||||
| chr3:32106410-32106750 | Common:4; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:32570623-32570937 | Rare:142 |