| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31442680-31443350 | Common:3; Rare:197 | ||||
| chr16:31457773-31458311 | Common:2; Rare:183 | ||||
| chr16:31458260-31458660 | Common:3; Rare:128 | ||||
| chr16:31458869-31459304 | Common:2; Rare:215 | ||||
| chr16:31459265-31459616 | Common:4; Rare:335 | ||||
| chr16:31471851-31472291 | Rare:194 | ||||
| chr16:31487570-31488070 | Common:3; Rare:303; Clinvar:3; Clinvar (pathogenic):3 | ||||
| chr16:31507860-31508270 | Common:4; Rare:231 | ||||
| chr16:31508293-31508589 | Common:12; Rare:295 | ||||
| chr16:31713049-31713408 | Common:2; Rare:151 | ||||
| chr16:31713515-31714000 | Common:2; Rare:157 | ||||
| chr16:31873639-31873931 | Common:1; Rare:96 | ||||
| chr16:46688695-46688807 | Rare:24 | ||||
| chr16:46689083-46689438 | Common:3; Rare:310; Clinvar:6; Clinvar (benign):3 | ||||
| chr16:46689444-46689801 | Common:7; Rare:322; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):3 |