| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31094568-31095050 | Common:1; Rare:148; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31108296-31108554 | Rare:60 | ||||
| chr16:31179820-31180151 | Common:1; Rare:120 | ||||
| chr16:31180596-31180835 | Common:3; Rare:88 | ||||
| chr16:31442745-31443064 | Common:1; Rare:53 | ||||
| chr16:31459091-31459164 | Rare:24 | ||||
| chr16:31459297-31459510 | Common:1; Rare:87 | ||||
| chr16:31471901-31472186 | Rare:64 | ||||
| chr16:31507814-31508053 | Common:1; Rare:87 | ||||
| chr16:31508365-31508516 | Common:4; Rare:64 | ||||
| chr16:46689115-46689422 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689454-46689744 | Common:3; Rare:113; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46690130-46690271 | Rare:32 | ||||
| chr16:46748224-46748564 | Rare:68 | ||||
| chr16:46763087-46763265 | Common:1; Rare:26 |