| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67537331-67537494 | Common:1; Rare:33 | ||||
| chr16:67666507-67666867 | Common:1; Rare:70 | ||||
| chr16:67842258-67842605 | Common:1; Rare:108 | ||||
| chr16:67843630-67843713 | Rare:12 | ||||
| chr16:68000565-68000722 | Rare:28 | ||||
| chr16:68023209-68023325 | Common:1; Rare:31 | ||||
| chr16:68310896-68311084 | Common:1; Rare:98 | ||||
| chr16:69132532-69132674 | Rare:57 | ||||
| chr16:69339548-69339810 | Rare:103; Clinvar (benign):1 | ||||
| chr16:69762247-69762379 | Common:1; Rare:38 | ||||
| chr16:70289440-70289802 | Common:3; Rare:146; Clinvar:1 | ||||
| chr16:70346781-70346957 | Common:1; Rare:88 | ||||
| chr16:70523524-70523847 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71894944-71895136 | Common:1; Rare:55 | ||||
| chr16:72093587-72093934 | Rare:86 |