| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4253745-4254094 | Common:4; Rare:137 | ||||
| chr16:4328291-4328406 | Rare:28 | ||||
| chr16:4380793-4380945 | Rare:46 | ||||
| chr16:4610780-4610902 | Rare:31 | ||||
| chr16:4682919-4683200 | Common:1; Rare:102 | ||||
| chr16:4797932-4798178 | Rare:137; Clinvar:13; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:4812224-4812352 | Rare:54 | ||||
| chr16:4819253-4819499 | Common:1; Rare:73 | ||||
| chr16:8806120-8806427 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chr16:8814254-8814352 | Common:1; Rare:14 | ||||
| chr16:8839381-8839832 | Common:2; Rare:118 | ||||
| chr16:10761493-10761795 | Common:1; Rare:86 | ||||
| chr16:10992718-10993057 | Common:1; Rare:80 | ||||
| chr16:11078134-11078259 | Common:3; Rare:15 | ||||
| chr16:11166525-11166833 | Common:1; Rare:92 |