| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49007006-49007429 | Common:2; Rare:146 | ||||
| chr3:49018544-49018604 | Rare:22 | ||||
| chr3:49021502-49021710 | Rare:52; Clinvar:1 | ||||
| chr3:49029384-49029716 | Common:2; Rare:176 | ||||
| chr3:49104711-49104910 | Rare:87; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49122294-49122424 | Rare:42; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:49132979-49133161 | Rare:38; Clinvar:1 | ||||
| chr3:49166289-49166422 | Common:1; Rare:35 | ||||
| chr3:49339998-49340270 | Common:3; Rare:97 | ||||
| chr3:49358121-49358458 | Common:4; Rare:175 | ||||
| chr3:49411878-49412432 | Common:2; Rare:203 | ||||
| chr3:49470007-49470319 | Common:1; Rare:91 | ||||
| chr3:49674228-49674395 | Common:1; Rare:62 | ||||
| chr3:49689460-49689597 | Rare:42 | ||||
| chr3:49723907-49724208 | Common:9; Rare:104 |