| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49093441-49093650 | Rare:73 | ||||
| chr3:49093911-49094145 | Rare:60 | ||||
| chr3:49104605-49104910 | Common:1; Rare:127; Clinvar:5; Clinvar (benign):7 | ||||
| chr3:49120754-49121005 | Rare:75 | ||||
| chr3:49133016-49133179 | Rare:33; Clinvar:1 | ||||
| chr3:49166284-49166394 | Common:1; Rare:31 | ||||
| chr3:49171292-49171636 | Common:3; Rare:69 | ||||
| chr3:49340013-49340308 | Common:3; Rare:100 | ||||
| chr3:49358255-49358486 | Common:3; Rare:125 | ||||
| chr3:49411867-49412432 | Common:2; Rare:206 | ||||
| chr3:49429223-49429461 | Common:1; Rare:56 | ||||
| chr3:49469964-49470325 | Common:1; Rare:115 | ||||
| chr3:49673546-49673859 | Common:2; Rare:64 | ||||
| chr3:49674218-49674402 | Common:1; Rare:71 | ||||
| chr3:49689440-49689662 | Rare:66 |