| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63551459-63551582 | Rare:27 | ||||
| chr14:63777128-63777299 | Common:1; Rare:26 | ||||
| chr14:63853571-63853685 | Rare:24 | ||||
| chr14:63853882-63854040 | Common:1; Rare:25 | ||||
| chr14:63854087-63854196 | Common:1; Rare:16 | ||||
| chr14:63996665-63996889 | Rare:42 | ||||
| chr14:63997039-63997116 | Rare:27; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:64338744-64339107 | Common:3; Rare:105 | ||||
| chr14:64445608-64445769 | Rare:29 | ||||
| chr14:64539519-64539690 | Common:2; Rare:48 | ||||
| chr14:64636810-64636939 | Rare:27 | ||||
| chr14:64637808-64637916 | Rare:18 | ||||
| chr14:64645354-64645404 | Rare:11 | ||||
| chr14:64645424-64645546 | Common:3; Rare:24 | ||||
| chr14:64645765-64645932 | Rare:24 |