| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31190077-31190340 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:31459331-31459517 | Common:1; Rare:76 | ||||
| chr16:46689124-46689376 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689521-46689720 | Common:2; Rare:85; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973632-46973811 | Rare:85 | ||||
| chr16:47461031-47461345 | Common:2; Rare:113; Clinvar (benign):2 | ||||
| chr16:53703821-53704220 | Common:1; Rare:126; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286722-54286969 | Common:1; Rare:71 | ||||
| chr16:56451102-56451697 | Common:4; Rare:198 | ||||
| chr16:56608324-56608766 | Common:4; Rare:126 | ||||
| chr16:56625589-56625839 | Common:1; Rare:77 | ||||
| chr16:56931862-56932163 | Common:3; Rare:132 | ||||
| chr16:56989381-56989577 | Common:1; Rare:45; Clinvar:1 | ||||
| chr16:57185959-57186339 | Common:1; Rare:110 | ||||
| chr16:57447356-57447508 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):1 |