| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73105836-73106283 | Common:2; Rare:116 | ||||
| chr14:73136942-73137302 | Common:1; Rare:66 | ||||
| chr14:73206458-73206731 | Common:2; Rare:35; Clinvar (benign):1 | ||||
| chr14:73458478-73458907 | Common:6; Rare:119 | ||||
| chr14:73536978-73537184 | Common:5; Rare:23 | ||||
| chr14:73568719-73569298 | Common:1; Rare:108 | ||||
| chr14:73760001-73760290 | Common:1; Rare:60 | ||||
| chr14:73787125-73787376 | Common:2; Rare:87 | ||||
| chr14:73857475-73857656 | Common:4; Rare:34 | ||||
| chr14:73950107-73950333 | Common:5; Rare:91; Clinvar (benign):3 | ||||
| chr14:74003660-74003690 | Rare:4 | ||||
| chr14:74019236-74019442 | Common:1; Rare:79 | ||||
| chr14:74084387-74084640 | Common:2; Rare:68 | ||||
| chr14:74302905-74303028 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr14:74493385-74493790 | Common:4; Rare:128; Clinvar (benign):4 |