| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49767975-49768164 | Common:2; Rare:68 | ||||
| chr14:49777695-49777873 | Rare:40 | ||||
| chr14:49892882-49893168 | Rare:123 | ||||
| chr14:50116473-50116752 | Common:1; Rare:143 | ||||
| chr14:50231063-50231192 | Common:2; Rare:47; Clinvar (benign):1 | ||||
| chr14:50312172-50312379 | Rare:88 | ||||
| chr14:50532451-50532632 | Common:3; Rare:51 | ||||
| chr14:50561120-50561198 | Rare:14 | ||||
| chr14:50668295-50668556 | Common:3; Rare:95 | ||||
| chr14:50944192-50944618 | Common:6; Rare:147; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr14:51239967-51240375 | Common:2; Rare:141 | ||||
| chr14:51554463-51554719 | Rare:51 | ||||
| chr14:51651656-51652025 | Common:4; Rare:109 | ||||
| chr14:51860681-51860769 | Rare:30 | ||||
| chr14:51989374-51989697 | Common:2; Rare:106 |