| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67935440-67936140 | Common:11; Rare:979 | ||||
| chr16:67936222-67936867 | Common:2; Rare:472 | ||||
| chr16:67936769-67936952 | Common:2; Rare:84 | ||||
| chr16:67936879-67937279 | Common:2; Rare:66 | ||||
| chr16:67943943-67944539 | Rare:242; Clinvar (pathogenic):2 | ||||
| chr16:67944990-67945390 | Rare:150 | ||||
| chr16:67950986-67951538 | Rare:200 | ||||
| chr16:67963649-67964049 | Common:3; Rare:109 | ||||
| chr16:67966656-67967056 | Rare:88 | ||||
| chr16:67967997-67968397 | Common:4; Rare:162 | ||||
| chr16:67968487-67968929 | Common:11; Rare:590 | ||||
| chr16:67969000-67969514 | Rare:290 | ||||
| chr16:67969530-67969956 | Common:3; Rare:190 | ||||
| chr16:67993219-67994197 | Common:13; Rare:581 | ||||
| chr16:67998770-67999170 | Common:5; Rare:181 |