| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31202580-31202873 | Common:2; Rare:107 | ||||
| chr16:31458018-31458339 | Common:1; Rare:72 | ||||
| chr16:31459324-31459510 | Common:1; Rare:77 | ||||
| chr16:31508365-31508470 | Common:1; Rare:44 | ||||
| chr16:46689125-46689437 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689489-46689716 | Common:2; Rare:93; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46884187-46884420 | Common:1; Rare:64 | ||||
| chr16:46959002-46959419 | Rare:113 | ||||
| chr16:46973600-46973789 | Rare:86 | ||||
| chr16:47143937-47144031 | Rare:39 | ||||
| chr16:47460840-47461421 | Common:3; Rare:229; Clinvar (benign):3 | ||||
| chr16:47461964-47462257 | Common:1; Rare:43 | ||||
| chr16:48244260-48244433 | Common:2; Rare:59 | ||||
| chr16:48365883-48365979 | Common:3; Rare:27 | ||||
| chr16:48385252-48385526 | Common:3; Rare:105 |