| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67935776-67935968 | Common:1; Rare:61 | ||||
| chr16:68023209-68023294 | Common:1; Rare:21 | ||||
| chr16:68245180-68245402 | Common:1; Rare:67 | ||||
| chr16:68310922-68311062 | Common:1; Rare:67 | ||||
| chr16:68539138-68539329 | Common:2; Rare:97 | ||||
| chr16:69132547-69132671 | Rare:52 | ||||
| chr16:69339562-69339799 | Rare:92; Clinvar (benign):1 | ||||
| chr16:69762273-69762367 | Common:1; Rare:23 | ||||
| chr16:70114127-70114369 | Common:3; Rare:88 | ||||
| chr16:70346744-70346937 | Common:1; Rare:93 | ||||
| chr16:70523539-70523829 | Common:3; Rare:90 | ||||
| chr16:71808782-71808869 | Common:1; Rare:50 | ||||
| chr16:71845874-71846023 | Common:2; Rare:53 | ||||
| chr16:71895254-71895550 | Common:2; Rare:107 | ||||
| chr16:72093605-72093929 | Rare:74 |