| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:55656560-55656650 | Rare:17 | ||||
| chr16:56191077-56191406 | Common:5; Rare:116 | ||||
| chr16:56451286-56451619 | Common:1; Rare:111 | ||||
| chr16:56519975-56520145 | Common:4; Rare:64; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56608266-56608662 | Common:3; Rare:108 | ||||
| chr16:56682298-56682521 | Common:4; Rare:78 | ||||
| chr16:56729945-56730216 | Common:1; Rare:67 | ||||
| chr16:56931867-56932181 | Common:3; Rare:146 | ||||
| chr16:57185724-57186433 | Common:4; Rare:200 | ||||
| chr16:57244956-57245279 | Common:3; Rare:107 | ||||
| chr16:57447340-57447514 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:57479747-57479969 | Common:1; Rare:36 | ||||
| chr16:57484112-57484299 | Rare:40 | ||||
| chr16:57639354-57639492 | Rare:29; Clinvar (pathogenic):1 | ||||
| chr16:57946471-57946706 | Rare:41 |