| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69566061-69566322 | Common:1; Rare:65 | ||||
| chr16:69726548-69726826 | Common:3; Rare:64 | ||||
| chr16:69762251-69762381 | Common:1; Rare:35 | ||||
| chr16:70114127-70114393 | Common:3; Rare:95 | ||||
| chr16:70289424-70289769 | Common:3; Rare:139; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:70346759-70346971 | Common:2; Rare:103 | ||||
| chr16:70523517-70523874 | Common:3; Rare:121; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70744586-70744728 | Common:1; Rare:38 | ||||
| chr16:71289313-71289668 | Common:3; Rare:118 | ||||
| chr16:71564930-71565016 | Rare:31 | ||||
| chr16:71576979-71577238 | Common:2; Rare:39; Clinvar (benign):2 | ||||
| chr16:71808774-71808875 | Common:1; Rare:58 | ||||
| chr16:71809028-71809323 | Common:3; Rare:95 | ||||
| chr16:71845895-71846023 | Common:2; Rare:41 | ||||
| chr16:71895313-71895584 | Common:3; Rare:100 |