| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689506-46689708 | Common:2; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46789925-46790093 | Common:4; Rare:41 | ||||
| chr16:46884067-46884415 | Common:2; Rare:99 | ||||
| chr16:46973532-46973781 | Rare:97 | ||||
| chr16:47460965-47461392 | Common:3; Rare:174; Clinvar (benign):3 | ||||
| chr16:48244254-48244621 | Common:2; Rare:107 | ||||
| chr16:48609979-48610311 | Common:2; Rare:117 | ||||
| chr16:50152865-50152943 | Rare:30 | ||||
| chr16:50245935-50246142 | Common:2; Rare:46 | ||||
| chr16:50319993-50320317 | Common:2; Rare:83 | ||||
| chr16:50693515-50693600 | Rare:34 | ||||
| chr16:50741708-50742162 | Common:7; Rare:135; Clinvar:1 | ||||
| chr16:50742704-50742782 | Rare:15 | ||||
| chr16:53054709-53055048 | Common:2; Rare:74 | ||||
| chr16:53099002-53099224 | Rare:42 |