| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:10876929-10877299 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:10878759-10879005 | Rare:53 | ||||
| chr16:10944321-10944680 | Common:1; Rare:116 | ||||
| chr16:11586896-11587107 | Common:3; Rare:55 | ||||
| chr16:11587166-11587246 | Common:1; Rare:14 | ||||
| chr16:11587395-11587419 | Rare:4 | ||||
| chr16:11629190-11629367 | Common:2; Rare:45 | ||||
| chr16:11742723-11743054 | Common:2; Rare:141 | ||||
| chr16:11797176-11797578 | Common:4; Rare:159 | ||||
| chr16:11851512-11851660 | Rare:74 | ||||
| chr16:11886930-11887073 | Common:1; Rare:40 | ||||
| chr16:11887092-11887227 | Rare:25 | ||||
| chr16:11915370-11915736 | Common:5; Rare:143 | ||||
| chr16:11915858-11916215 | Common:2; Rare:144 | ||||
| chr16:11976609-11976789 | Common:3; Rare:74 |