| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68265299-68265566 | Common:1; Rare:42 | ||||
| chr16:68310911-68311081 | Common:1; Rare:87 | ||||
| chr16:69132532-69132671 | Rare:56 | ||||
| chr16:69339548-69339821 | Common:1; Rare:110; Clinvar (benign):1 | ||||
| chr16:69726421-69726727 | Common:4; Rare:86 | ||||
| chr16:69762279-69762367 | Common:1; Rare:21 | ||||
| chr16:70114152-70114369 | Common:2; Rare:77 | ||||
| chr16:70454521-70454612 | Common:1; Rare:29 | ||||
| chr16:70523527-70523837 | Common:3; Rare:100; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:71808774-71808869 | Common:1; Rare:53 | ||||
| chr16:71809053-71809155 | Rare:46 | ||||
| chr16:71895241-71895578 | Common:3; Rare:132 | ||||
| chr16:72013933-72014470 | Common:4; Rare:118 | ||||
| chr16:72093574-72093957 | Rare:97 | ||||
| chr16:74296460-74296920 | Common:1; Rare:153 |