| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69726446-69726768 | Common:3; Rare:82 | ||||
| chr16:70114138-70114393 | Common:2; Rare:89 | ||||
| chr16:70346759-70347042 | Common:2; Rare:128 | ||||
| chr16:70454347-70454619 | Common:1; Rare:71 | ||||
| chr16:70523512-70523844 | Common:3; Rare:112; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71808761-71808885 | Common:1; Rare:65 | ||||
| chr16:71808979-71809323 | Common:3; Rare:115 | ||||
| chr16:71845890-71846029 | Common:2; Rare:45 | ||||
| chr16:71895250-71895584 | Common:3; Rare:129 | ||||
| chr16:72008500-72008765 | Common:5; Rare:100; Clinvar (benign):1 | ||||
| chr16:72093597-72093940 | Rare:81 | ||||
| chr16:74296719-74296988 | Rare:107 | ||||
| chr16:75433373-75433812 | Common:4; Rare:138 | ||||
| chr16:75566222-75566446 | Common:1; Rare:113 | ||||
| chr16:75647584-75647844 | Common:2; Rare:128; Clinvar:4; Clinvar (pathogenic):1 |