| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100239931-100240286 | Common:2; Rare:126 | ||||
| chr14:100305408-100305716 | Common:4; Rare:74 | ||||
| chr14:100306429-100306763 | Common:3; Rare:122 | ||||
| chr14:100306858-100306942 | Common:1; Rare:30 | ||||
| chr14:100374751-100375056 | Common:2; Rare:50 | ||||
| chr14:100375432-100375942 | Common:2; Rare:78 | ||||
| chr14:100376059-100376620 | Common:5; Rare:152 | ||||
| chr14:101761378-101761819 | Common:8; Rare:116 | ||||
| chr14:101809634-101809970 | Rare:71 | ||||
| chr14:101810152-101810462 | Common:2; Rare:57 | ||||
| chr14:101964288-101964710 | Common:5; Rare:126; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:102086433-102086646 | Common:3; Rare:104 | ||||
| chr14:102086907-102087483 | Common:9; Rare:234 | ||||
| chr14:102087519-102087733 | Common:1; Rare:73 | ||||
| chr14:102139250-102139449 | Rare:87 |