| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67660222-67660409 | Rare:118; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67660793-67661052 | Common:2; Rare:90 | ||||
| chr16:67719185-67719451 | Rare:63 | ||||
| chr16:67806532-67806878 | Rare:68 | ||||
| chr16:67846779-67846983 | Common:1; Rare:56 | ||||
| chr16:67893046-67893254 | Common:2; Rare:56 | ||||
| chr16:67935628-67935959 | Common:1; Rare:111 | ||||
| chr16:67998845-67999060 | Common:1; Rare:45 | ||||
| chr16:68023207-68023335 | Common:1; Rare:35 | ||||
| chr16:68084677-68084824 | Rare:30 | ||||
| chr16:68245129-68245402 | Common:1; Rare:80 | ||||
| chr16:68264430-68264569 | Rare:48 | ||||
| chr16:68310858-68311170 | Common:3; Rare:150 | ||||
| chr16:68530038-68530155 | Common:4; Rare:52 | ||||
| chr16:68539169-68539385 | Common:2; Rare:96 |