| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50944916-50945080 | Common:2; Rare:58 | ||||
| chr14:50945100-50945510 | Common:6; Rare:125 | ||||
| chr14:51095071-51095390 | Common:8; Rare:239 | ||||
| chr14:51239981-51240307 | Common:2; Rare:111 | ||||
| chr14:51651410-51652090 | Common:10; Rare:340 | ||||
| chr14:51989376-51989637 | Common:4; Rare:156 | ||||
| chr14:52552447-52552836 | Common:2; Rare:236 | ||||
| chr14:52695488-52695839 | Common:2; Rare:176 | ||||
| chr14:52695866-52695992 | Common:1; Rare:57 | ||||
| chr14:52707045-52707229 | Common:2; Rare:156 | ||||
| chr14:52791423-52791856 | Common:4; Rare:260 | ||||
| chr14:52951003-52951444 | Common:8; Rare:301 | ||||
| chr14:53152200-53152760 | Common:3; Rare:345; Clinvar:1; Clinvar (benign):7 | ||||
| chr14:53153155-53153600 | Common:5; Rare:210 | ||||
| chr14:53953366-53953645 | Common:4; Rare:150 |