| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73644883-73645034 | Common:5; Rare:83; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:73713840-73714240 | Common:1; Rare:157 | ||||
| chr14:73759990-73760760 | Common:6; Rare:210 | ||||
| chr14:73787125-73787300 | Common:2; Rare:123 | ||||
| chr14:73851595-73852030 | Common:10; Rare:206 | ||||
| chr14:73949690-73949960 | Common:7; Rare:109 | ||||
| chr14:73950053-73950333 | Common:11; Rare:222; Clinvar (benign):7 | ||||
| chr14:73950500-73950820 | Common:3; Rare:142; Clinvar (benign):1 | ||||
| chr14:74019122-74019432 | Common:4; Rare:184 | ||||
| chr14:74084384-74084786 | Common:13; Rare:178 | ||||
| chr14:74302921-74303137 | Common:2; Rare:146; Clinvar (benign):2 | ||||
| chr14:74493233-74493781 | Common:7; Rare:252; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr14:74712994-74713228 | Common:1; Rare:219 | ||||
| chr14:74763070-74763448 | Rare:195 | ||||
| chr14:74881778-74882015 | Common:1; Rare:163 |