| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73463554-73463804 | Common:1; Rare:43 | ||||
| chr14:73568511-73568822 | Common:4; Rare:64 | ||||
| chr14:73569061-73569312 | Rare:65 | ||||
| chr14:73644935-73645041 | Common:1; Rare:31; Clinvar:2 | ||||
| chr14:73714358-73714569 | Common:2; Rare:74 | ||||
| chr14:73787125-73787371 | Common:2; Rare:87 | ||||
| chr14:73790084-73790392 | Common:2; Rare:50 | ||||
| chr14:73851592-73852023 | Common:6; Rare:120 | ||||
| chr14:73950107-73950335 | Common:5; Rare:93; Clinvar (benign):3 | ||||
| chr14:74019221-74019467 | Common:2; Rare:92 | ||||
| chr14:74084397-74084597 | Common:2; Rare:57 | ||||
| chr14:74302914-74303098 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr14:74492642-74492880 | Common:2; Rare:45 | ||||
| chr14:74493219-74493810 | Common:4; Rare:200; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:74611578-74611627 | Rare:14 |