| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31074192-31074456 | Common:1; Rare:74 | ||||
| chr16:31471901-31472205 | Rare:71 | ||||
| chr16:31508339-31508457 | Common:1; Rare:54 | ||||
| chr16:46689134-46689317 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689516-46689709 | Common:2; Rare:79; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973626-46973772 | Rare:70 | ||||
| chr16:47460840-47461383 | Common:2; Rare:215; Clinvar (benign):2 | ||||
| chr16:48385258-48385565 | Common:3; Rare:121 | ||||
| chr16:48610133-48610310 | Common:2; Rare:76 | ||||
| chr16:51151242-51151316 | Common:1; Rare:17 | ||||
| chr16:53703821-53704213 | Common:1; Rare:123; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:55479123-55479422 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:56451145-56451697 | Common:4; Rare:185 | ||||
| chr16:56608443-56608804 | Common:3; Rare:104 | ||||
| chr16:56625666-56625833 | Rare:49 |