| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:635280-635851 | Common:7; Rare:178 | ||||
| chr16:636094-636475 | Common:4; Rare:112 | ||||
| chr16:641744-642040 | Common:3; Rare:102 | ||||
| chr16:647128-647542 | Rare:132 | ||||
| chr16:660892-661085 | Common:22; Rare:107 | ||||
| chr16:679745-680174 | Common:8; Rare:114 | ||||
| chr16:680374-680699 | Common:1; Rare:98 | ||||
| chr16:681141-681619 | Rare:161; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr16:684065-684595 | Common:3; Rare:272 | ||||
| chr16:720477-720599 | Common:1; Rare:31 | ||||
| chr16:721047-721251 | Common:4; Rare:60 | ||||
| chr16:721375-721573 | Common:2; Rare:70 | ||||
| chr16:726877-727346 | Common:7; Rare:127 | ||||
| chr16:740919-741161 | Common:1; Rare:79 | ||||
| chr16:1314016-1314376 | Common:6; Rare:108 |