| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31074126-31074509 | Common:3; Rare:108 | ||||
| chr16:31074605-31074938 | Common:3; Rare:64 | ||||
| chr16:31094628-31094798 | Common:1; Rare:70; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:31094841-31095040 | Rare:47; Clinvar:1 | ||||
| chr16:31095995-31096104 | Rare:18 | ||||
| chr16:31108275-31108460 | Rare:40 | ||||
| chr16:31117446-31117760 | Common:2; Rare:91 | ||||
| chr16:31117838-31118099 | Rare:61 | ||||
| chr16:31142178-31142661 | Common:3; Rare:132 | ||||
| chr16:31179723-31180428 | Common:4; Rare:288; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:31180540-31180872 | Common:3; Rare:123 | ||||
| chr16:31187925-31188093 | Common:1; Rare:32 | ||||
| chr16:31442633-31442673 | Rare:5 | ||||
| chr16:31442703-31443188 | Common:2; Rare:97 | ||||
| chr16:31458174-31458377 | Common:1; Rare:60 |