| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46972981-46973065 | Rare:28 | ||||
| chr16:46973570-46973873 | Rare:133 | ||||
| chr16:46973965-46974075 | Common:3; Rare:21 | ||||
| chr16:47143088-47143265 | Rare:33 | ||||
| chr16:47143412-47143646 | Common:1; Rare:63 | ||||
| chr16:47143891-47144145 | Rare:117 | ||||
| chr16:47460831-47461418 | Common:3; Rare:230; Clinvar (benign):3 | ||||
| chr16:47461706-47461828 | Rare:26 | ||||
| chr16:47462048-47462200 | Rare:17 | ||||
| chr16:48244182-48244492 | Common:3; Rare:98 | ||||
| chr16:48365753-48366072 | Common:5; Rare:88 | ||||
| chr16:48366076-48366312 | Rare:55 | ||||
| chr16:48385068-48385207 | Rare:37 | ||||
| chr16:48385245-48385669 | Common:3; Rare:162 | ||||
| chr16:48609848-48609971 | Rare:42 |