| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30949187-30949295 | Common:2; Rare:38 | ||||
| chr16:31074187-31074457 | Common:1; Rare:75 | ||||
| chr16:31094725-31095050 | Rare:87; Clinvar:1 | ||||
| chr16:31108300-31108458 | Rare:39 | ||||
| chr16:31179851-31180144 | Common:1; Rare:106 | ||||
| chr16:31442769-31443059 | Common:1; Rare:47 | ||||
| chr16:31471931-31472208 | Rare:65 | ||||
| chr16:31508374-31508478 | Common:1; Rare:41 | ||||
| chr16:46689134-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689465-46689708 | Common:2; Rare:90; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973626-46973757 | Rare:62 | ||||
| chr16:47461032-47461365 | Common:2; Rare:124; Clinvar (benign):2 | ||||
| chr16:48385302-48385562 | Common:3; Rare:106 | ||||
| chr16:50266422-50266561 | Common:1; Rare:39 | ||||
| chr16:53054959-53055048 | Rare:16 |