| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49021503-49021720 | Rare:55; Clinvar:1 | ||||
| chr3:49022072-49022183 | Rare:48; Clinvar (pathogenic):1 | ||||
| chr3:49025143-49025438 | Common:1; Rare:64 | ||||
| chr3:49029365-49029477 | Common:1; Rare:82 | ||||
| chr3:49093595-49093670 | Rare:33 | ||||
| chr3:49104615-49104910 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120754-49121137 | Rare:106; Clinvar:1 | ||||
| chr3:49125422-49125529 | Rare:33 | ||||
| chr3:49132831-49133170 | Rare:76; Clinvar:3 | ||||
| chr3:49166294-49166437 | Common:1; Rare:35 | ||||
| chr3:49171480-49171642 | Common:2; Rare:37 | ||||
| chr3:49276935-49277178 | Common:2; Rare:86 | ||||
| chr3:49340003-49340294 | Common:3; Rare:101 | ||||
| chr3:49411882-49412423 | Common:2; Rare:197 | ||||
| chr3:49429246-49429420 | Rare:43 |