| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63853810-63854210 | Common:2; Rare:73 | ||||
| chr14:64216039-64216268 | Common:1; Rare:75; Clinvar (benign):4 | ||||
| chr14:64338786-64339158 | Common:5; Rare:100 | ||||
| chr14:64466057-64466175 | Rare:19 | ||||
| chr14:64501513-64502187 | Common:2; Rare:215 | ||||
| chr14:64538740-64539377 | Common:4; Rare:167 | ||||
| chr14:64539485-64539654 | Common:3; Rare:105 | ||||
| chr14:64625410-64625788 | Common:4; Rare:142 | ||||
| chr14:64703154-64703435 | Rare:97 | ||||
| chr14:64705400-64705770 | Rare:114 | ||||
| chr14:64719970-64720701 | Common:5; Rare:279 | ||||
| chr14:64806431-64806773 | Common:2; Rare:50 | ||||
| chr14:64880443-64880656 | Common:2; Rare:41 | ||||
| chr14:64966830-64967265 | Common:2; Rare:153 | ||||
| chr14:65095738-65096039 | Common:2; Rare:58 |