| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68539158-68539373 | Common:2; Rare:97 | ||||
| chr16:69132537-69132689 | Rare:62 | ||||
| chr16:69339562-69339823 | Common:1; Rare:105; Clinvar (benign):1 | ||||
| chr16:69424404-69424686 | Common:1; Rare:78 | ||||
| chr16:69726431-69726782 | Common:4; Rare:93 | ||||
| chr16:69754900-69755052 | Rare:58 | ||||
| chr16:69762266-69762367 | Common:1; Rare:24 | ||||
| chr16:70114105-70114376 | Common:3; Rare:94 | ||||
| chr16:70289440-70289770 | Common:3; Rare:135; Clinvar:1 | ||||
| chr16:70299093-70299230 | Common:1; Rare:29 | ||||
| chr16:70346763-70346965 | Common:1; Rare:100 | ||||
| chr16:70523532-70523855 | Common:3; Rare:105; Clinvar (pathogenic):1 | ||||
| chr16:71564926-71565006 | Rare:28 | ||||
| chr16:71808761-71809129 | Common:1; Rare:156 | ||||
| chr16:71845920-71846023 | Common:1; Rare:33 |