| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48662999-48663042 | Rare:14 | ||||
| chr3:48847717-48847965 | Common:1; Rare:70 | ||||
| chr3:48918754-48918986 | Common:2; Rare:133 | ||||
| chr3:48989738-48989892 | Rare:40 | ||||
| chr3:49007194-49007627 | Common:2; Rare:151 | ||||
| chr3:49007804-49008047 | Common:2; Rare:66 | ||||
| chr3:49021490-49021813 | Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:49022011-49022204 | Rare:69; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49022380-49023110 | Common:2; Rare:273; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):5 | ||||
| chr3:49029259-49029533 | Common:2; Rare:161 | ||||
| chr3:49092878-49093153 | Common:1; Rare:70 | ||||
| chr3:49093554-49093743 | Common:1; Rare:71 | ||||
| chr3:49093914-49094085 | Rare:49 | ||||
| chr3:49094346-49094588 | Common:2; Rare:63 | ||||
| chr3:49104623-49104913 | Common:1; Rare:119; Clinvar:3; Clinvar (benign):7 |