| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49007160-49007429 | Common:2; Rare:110 | ||||
| chr3:49018552-49018633 | Rare:29 | ||||
| chr3:49021502-49021710 | Rare:52; Clinvar:1 | ||||
| chr3:49021993-49022154 | Rare:53; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49029334-49029482 | Common:1; Rare:103 | ||||
| chr3:49093469-49093670 | Rare:77 | ||||
| chr3:49104726-49104910 | Rare:77; Clinvar (benign):3 | ||||
| chr3:49132824-49133100 | Rare:64; Clinvar:2 | ||||
| chr3:49171480-49171636 | Common:2; Rare:36 | ||||
| chr3:49358267-49358486 | Common:2; Rare:119 | ||||
| chr3:49411839-49412355 | Common:2; Rare:178 | ||||
| chr3:49429255-49429461 | Common:1; Rare:44 | ||||
| chr3:49674228-49674398 | Common:1; Rare:64 | ||||
| chr3:49689460-49689606 | Rare:46 | ||||
| chr3:49723895-49724164 | Common:6; Rare:87 |