| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31508374-31508481 | Common:2; Rare:41 | ||||
| chr16:46689116-46689376 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689516-46689716 | Common:2; Rare:84; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973638-46973774 | Rare:65 | ||||
| chr16:47461051-47461350 | Common:2; Rare:102; Clinvar (benign):2 | ||||
| chr16:50245926-50246184 | Common:2; Rare:60 | ||||
| chr16:53703810-53704223 | Common:1; Rare:131; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286722-54287000 | Common:1; Rare:83 | ||||
| chr16:55478868-55479255 | Common:1; Rare:79 | ||||
| chr16:56451103-56451761 | Common:5; Rare:216 | ||||
| chr16:56608494-56608880 | Common:2; Rare:103 | ||||
| chr16:56625646-56626195 | Common:1; Rare:146 | ||||
| chr16:56931942-56932153 | Common:1; Rare:105 | ||||
| chr16:57185964-57186342 | Common:1; Rare:109 | ||||
| chr16:57244970-57245358 | Common:3; Rare:131 |