| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58629486-58629702 | Common:2; Rare:46 | ||||
| chr16:58629730-58630226 | Common:3; Rare:140 | ||||
| chr16:58630302-58630612 | Common:1; Rare:73 | ||||
| chr16:58684689-58684880 | Common:1; Rare:51 | ||||
| chr16:58733796-58733951 | Common:2; Rare:29 | ||||
| chr16:58734066-58734509 | Common:6; Rare:128 | ||||
| chr16:61918124-61918299 | Common:1; Rare:36 | ||||
| chr16:65122053-65122210 | Common:1; Rare:52 | ||||
| chr16:66426818-66426938 | Rare:26 | ||||
| chr16:66426965-66427258 | Common:1; Rare:93 | ||||
| chr16:66427302-66427346 | Rare:7 | ||||
| chr16:66516821-66517172 | Rare:66; Clinvar (pathogenic):2 | ||||
| chr16:66549193-66549365 | Rare:52 | ||||
| chr16:66549392-66549495 | Rare:24 | ||||
| chr16:66549549-66550319 | Common:7; Rare:282; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 |