| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39267100-39267422 | Common:1; Rare:114 | ||||
| chr14:39432453-39432637 | Common:6; Rare:64 | ||||
| chr14:41607278-41607385 | Common:1; Rare:24 | ||||
| chr14:44961898-44962243 | Common:3; Rare:98 | ||||
| chr14:49586342-49586732 | Common:1; Rare:205 | ||||
| chr14:49598862-49599023 | Common:1; Rare:60 | ||||
| chr14:49620573-49620827 | Common:2; Rare:102; Clinvar:3 | ||||
| chr14:49688199-49688287 | Rare:32 | ||||
| chr14:49892909-49893121 | Rare:84 | ||||
| chr14:50116541-50116696 | Rare:75 | ||||
| chr14:50312155-50312374 | Rare:93 | ||||
| chr14:50668326-50668556 | Common:3; Rare:85 | ||||
| chr14:50944405-50944567 | Common:4; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51239988-51240295 | Common:2; Rare:101 | ||||
| chr14:51989367-51989634 | Common:2; Rare:81 |