| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31487737-31488078 | Common:1; Rare:104; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:31488314-31488339 | Rare:4 | ||||
| chr16:31508274-31508459 | Common:1; Rare:84 | ||||
| chr16:31527863-31528184 | Common:2; Rare:73 | ||||
| chr16:46689111-46689317 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689498-46689732 | Common:2; Rare:102; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46884187-46884457 | Common:1; Rare:71 | ||||
| chr16:46915147-46915310 | Rare:36 | ||||
| chr16:46973585-46973801 | Rare:98 | ||||
| chr16:47461035-47461371 | Common:2; Rare:126; Clinvar (benign):2 | ||||
| chr16:48244190-48244411 | Common:2; Rare:76 | ||||
| chr16:48365883-48366093 | Common:5; Rare:63 | ||||
| chr16:48384789-48385057 | Common:3; Rare:99 | ||||
| chr16:48385230-48385593 | Common:3; Rare:136 | ||||
| chr16:48610125-48610388 | Common:3; Rare:96 |