| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46830599-46830999 | Common:2; Rare:144 | ||||
| chr16:46831113-46831307 | Common:2; Rare:77 | ||||
| chr16:46884073-46884401 | Common:2; Rare:93 | ||||
| chr16:46884432-46885186 | Common:5; Rare:238; Clinvar (pathogenic):2 | ||||
| chr16:46972555-46972680 | Rare:31 | ||||
| chr16:46973627-46973857 | Rare:105 | ||||
| chr16:47143054-47143244 | Rare:41 | ||||
| chr16:47143442-47143584 | Rare:42 | ||||
| chr16:47143933-47144144 | Rare:97 | ||||
| chr16:47460968-47461398 | Common:3; Rare:176; Clinvar (benign):3 | ||||
| chr16:47464033-47464433 | Common:1; Rare:76 | ||||
| chr16:48244184-48244344 | Common:2; Rare:50 | ||||
| chr16:48365879-48365979 | Common:3; Rare:29 | ||||
| chr16:48385405-48385679 | Common:1; Rare:103 | ||||
| chr16:48610122-48610384 | Common:3; Rare:94 |