| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:21191976-21192059 | Rare:12 | ||||
| chr14:22477868-22478057 | Common:2; Rare:50 | ||||
| chr14:22556178-22556745 | Common:10; Rare:118 | ||||
| chr14:22557303-22557437 | Common:6; Rare:33 | ||||
| chr14:24006876-24007116 | Common:1; Rare:67 | ||||
| chr14:32980645-32980817 | Common:1; Rare:31 | ||||
| chr14:35856205-35856393 | Rare:29 | ||||
| chr14:38125455-38125622 | Rare:26 | ||||
| chr14:38127412-38127642 | Common:1; Rare:38 | ||||
| chr14:49633866-49634070 | Common:1; Rare:74; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr14:49862689-49863054 | Common:1; Rare:162 | ||||
| chr14:49868124-49868398 | Common:2; Rare:62 | ||||
| chr14:49971291-49971418 | Rare:26 | ||||
| chr14:49972257-49972454 | Common:1; Rare:34 | ||||
| chr14:49977138-49977314 | Common:1; Rare:28 |