| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30650827-30651002 | Rare:57 | ||||
| chr16:30748128-30748441 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:30893940-30894259 | Common:5; Rare:87 | ||||
| chr16:30923264-30923603 | Common:1; Rare:75 | ||||
| chr16:31033307-31033592 | Common:2; Rare:95 | ||||
| chr16:31074182-31074456 | Common:2; Rare:75 | ||||
| chr16:31202667-31203007 | Common:2; Rare:116 | ||||
| chr16:31472109-31472431 | Common:1; Rare:70 | ||||
| chr16:31508374-31508470 | Common:1; Rare:38 | ||||
| chr16:46689134-46689295 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973581-46973781 | Rare:87 | ||||
| chr16:47461032-47461374 | Common:2; Rare:132; Clinvar (benign):2 | ||||
| chr16:48244264-48244400 | Common:2; Rare:46 | ||||
| chr16:53054827-53055055 | Common:2; Rare:54 | ||||
| chr16:53703815-53704203 | Common:1; Rare:120; Clinvar:4; Clinvar (benign):2 |