| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:44967564-44967607 | Rare:10 | ||||
| chr14:45084693-45084713 | Rare:3 | ||||
| chr14:45085186-45085265 | Common:1; Rare:16 | ||||
| chr14:45110649-45110887 | Rare:43 | ||||
| chr14:47269786-47269992 | Common:1; Rare:40 | ||||
| chr14:48617050-48617243 | Rare:32 | ||||
| chr14:48617449-48617506 | Rare:12 | ||||
| chr14:48936483-48936648 | Common:1; Rare:31 | ||||
| chr14:49585361-49585431 | Common:3; Rare:18 | ||||
| chr14:49633657-49633718 | Common:1; Rare:27; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:49633934-49634524 | Common:2; Rare:266; Clinvar:19; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr14:49687353-49687624 | Rare:56 | ||||
| chr14:49851672-49851994 | Common:1; Rare:84 | ||||
| chr14:49853912-49854066 | Rare:17 | ||||
| chr14:49861374-49861654 | Rare:45 |