| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:192917701-192918550 | Common:3; Rare:340 | ||||
| chr3:193593046-193593414 | Rare:207; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:194135983-194136188 | Rare:75 | ||||
| chr3:194486778-194487175 | Common:9; Rare:296 | ||||
| chr3:194633233-194633610 | Common:6; Rare:158 | ||||
| chr3:194672078-194672234 | Rare:84 | ||||
| chr3:194672370-194672640 | Common:6; Rare:114 | ||||
| chr3:195259940-195260320 | Common:3; Rare:112 | ||||
| chr3:195270640-195270990 | Rare:178 | ||||
| chr3:195271056-195271277 | Common:2; Rare:169 | ||||
| chr3:195442200-195442530 | Common:1; Rare:119 | ||||
| chr3:195442917-195443419 | Common:7; Rare:217 | ||||
| chr3:195543191-195543497 | Common:6; Rare:211 | ||||
| chr3:195876662-195876932 | Common:6; Rare:194 | ||||
| chr3:195895160-195895570 | Common:6; Rare:242 |