| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68539116-68539385 | Common:3; Rare:117 | ||||
| chr16:68539646-68539771 | Common:2; Rare:53 | ||||
| chr16:68843518-68843842 | Common:1; Rare:107 | ||||
| chr16:68843949-68844112 | Rare:34 | ||||
| chr16:69132130-69132420 | Rare:53 | ||||
| chr16:69132495-69132912 | Rare:128 | ||||
| chr16:69186582-69186793 | Common:1; Rare:31 | ||||
| chr16:69186937-69187225 | Rare:93 | ||||
| chr16:69187587-69187819 | Common:1; Rare:51 | ||||
| chr16:69311001-69311453 | Common:1; Rare:123 | ||||
| chr16:69330061-69330225 | Common:3; Rare:86 | ||||
| chr16:69330475-69330900 | Common:3; Rare:187; Clinvar (benign):2 | ||||
| chr16:69339220-69339370 | Rare:56; Clinvar:1 | ||||
| chr16:69339415-69339868 | Common:2; Rare:196; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:69385832-69386163 | Rare:111 |