| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48662893-48663037 | Rare:31 | ||||
| chr3:48847667-48847973 | Common:1; Rare:86 | ||||
| chr3:48918702-48918930 | Common:2; Rare:119 | ||||
| chr3:49007192-49007425 | Common:2; Rare:92 | ||||
| chr3:49018560-49018654 | Rare:31 | ||||
| chr3:49021502-49021710 | Rare:52; Clinvar:1 | ||||
| chr3:49021993-49022204 | Rare:75; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49102210-49102453 | Rare:71; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:49104615-49104910 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120754-49120976 | Rare:72 | ||||
| chr3:49132985-49133142 | Rare:34; Clinvar:1 | ||||
| chr3:49166284-49166387 | Common:1; Rare:30 | ||||
| chr3:49171450-49171597 | Rare:31 | ||||
| chr3:49277035-49277193 | Common:1; Rare:62 | ||||
| chr3:49339998-49340132 | Common:2; Rare:62 |