| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31190075-31190399 | Common:1; Rare:92; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:31202270-31202449 | Common:2; Rare:53 | ||||
| chr16:31202734-31202984 | Common:2; Rare:82 | ||||
| chr16:31508371-31508481 | Common:2; Rare:42 | ||||
| chr16:46689116-46689426 | Common:1; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689524-46689724 | Common:2; Rare:87; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46972953-46972998 | Common:1; Rare:15 | ||||
| chr16:46973591-46973802 | Rare:97 | ||||
| chr16:47461055-47461343 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chr16:48610184-48610391 | Common:3; Rare:73 | ||||
| chr16:50152862-50152939 | Rare:29 | ||||
| chr16:50681221-50681406 | Common:1; Rare:39 | ||||
| chr16:50742715-50742911 | Rare:33 | ||||
| chr16:53703825-53704199 | Rare:114; Clinvar:4 | ||||
| chr16:56451257-56451705 | Common:2; Rare:146 |