| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:29926178-29926309 | Common:2; Rare:50 | ||||
| chr16:29973742-29973924 | Common:2; Rare:78 | ||||
| chr16:29996070-29996289 | Common:2; Rare:79 | ||||
| chr16:30064375-30064485 | Rare:21; Clinvar (benign):1 | ||||
| chr16:30923253-30923588 | Common:1; Rare:82 | ||||
| chr16:31074213-31074456 | Common:1; Rare:66 | ||||
| chr16:31459335-31459512 | Common:1; Rare:74 | ||||
| chr16:46689134-46689419 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689524-46689706 | Common:2; Rare:77; Clinvar (benign):2 | ||||
| chr16:46973631-46973749 | Rare:57 | ||||
| chr16:47461051-47461351 | Common:2; Rare:103; Clinvar (benign):2 | ||||
| chr16:48244240-48244360 | Common:1; Rare:37 | ||||
| chr16:50245917-50246186 | Common:2; Rare:63 | ||||
| chr16:53703836-53704227 | Common:1; Rare:121; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:54286699-54287007 | Common:2; Rare:91 |