| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63542647-63543047 | Common:5; Rare:95 | ||||
| chr14:63543259-63543743 | Common:30; Rare:707 | ||||
| chr14:63641088-63641488 | Common:5; Rare:108 | ||||
| chr14:63641472-63642239 | Common:36; Rare:847 | ||||
| chr14:63642250-63642650 | Common:7; Rare:178 | ||||
| chr14:63727130-63727810 | Common:2; Rare:204 | ||||
| chr14:63727830-63728360 | Common:8; Rare:458 | ||||
| chr14:63852770-63853000 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:64293524-64294306 | Common:8; Rare:398 | ||||
| chr14:64294370-64294770 | Common:2; Rare:105 | ||||
| chr14:64337666-64338074 | Common:5; Rare:167 | ||||
| chr14:64338077-64339088 | Common:33; Rare:883 | ||||
| chr14:64387721-64388418 | Common:13; Rare:1011 | ||||
| chr14:64388483-64388956 | Common:4; Rare:171 | ||||
| chr14:64465206-64465631 | Common:6; Rare:337 |