| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66516978-66517138 | Rare:28 | ||||
| chr16:66549280-66549605 | Rare:88 | ||||
| chr16:66549679-66550206 | Common:7; Rare:216; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr16:66551502-66551635 | Rare:26 | ||||
| chr16:66552430-66552683 | Rare:108 | ||||
| chr16:66603879-66604007 | Rare:19 | ||||
| chr16:66604180-66604380 | Common:3; Rare:32 | ||||
| chr16:66604513-66604762 | Rare:68 | ||||
| chr16:66604874-66605015 | Common:1; Rare:51 | ||||
| chr16:66696016-66696208 | Rare:40 | ||||
| chr16:66696267-66696611 | Common:2; Rare:82 | ||||
| chr16:66696613-66697066 | Common:5; Rare:156 | ||||
| chr16:66697204-66697245 | Rare:10 | ||||
| chr16:66751130-66751302 | Rare:50 | ||||
| chr16:66751544-66751635 | Common:1; Rare:47 |