| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67481088-67481380 | Common:1; Rare:107 | ||||
| chr16:67660222-67660367 | Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67719286-67719474 | Common:1; Rare:51 | ||||
| chr16:67935661-67935953 | Common:1; Rare:92 | ||||
| chr16:67968557-67968863 | Common:2; Rare:105 | ||||
| chr16:68023207-68023337 | Common:1; Rare:35 | ||||
| chr16:68234156-68234477 | Rare:59 | ||||
| chr16:68235737-68235886 | Rare:51 | ||||
| chr16:68245187-68245410 | Common:1; Rare:71 | ||||
| chr16:68264430-68264564 | Rare:46 | ||||
| chr16:68310922-68311095 | Common:1; Rare:88 | ||||
| chr16:68539202-68539323 | Common:1; Rare:63 | ||||
| chr16:68808525-68808791 | Common:2; Rare:64; Clinvar:15; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr16:69132504-69132671 | Rare:61 | ||||
| chr16:69339399-69339826 | Common:2; Rare:180; Clinvar:1; Clinvar (benign):5 |