| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30893927-30894300 | Common:5; Rare:102 | ||||
| chr16:30896424-30896630 | Common:2; Rare:48 | ||||
| chr16:30923236-30923608 | Common:1; Rare:88 | ||||
| chr16:31033460-31033616 | Common:1; Rare:57 | ||||
| chr16:31074184-31074456 | Common:1; Rare:75 | ||||
| chr16:31108327-31108471 | Rare:37 | ||||
| chr16:31179820-31180158 | Common:1; Rare:129 | ||||
| chr16:31428074-31428473 | Common:4; Rare:130 | ||||
| chr16:31428496-31428531 | Rare:6 | ||||
| chr16:31442744-31443059 | Common:1; Rare:53 | ||||
| chr16:31458897-31459161 | Rare:76 | ||||
| chr16:31471896-31472200 | Rare:69 | ||||
| chr16:31508357-31508516 | Common:4; Rare:69 | ||||
| chr16:46689115-46689416 | Common:1; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689465-46689708 | Common:2; Rare:90; Clinvar (benign):2; Clinvar (pathogenic):1 |