| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69726549-69726806 | Common:3; Rare:59 | ||||
| chr16:69762230-69762384 | Common:1; Rare:41 | ||||
| chr16:70114118-70114407 | Common:3; Rare:101 | ||||
| chr16:70289419-70289579 | Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:70299142-70299249 | Rare:24 | ||||
| chr16:70346810-70346971 | Common:2; Rare:80 | ||||
| chr16:70523530-70523861 | Common:3; Rare:107; Clinvar (pathogenic):1 | ||||
| chr16:71462156-71462278 | Common:2; Rare:58 | ||||
| chr16:71809045-71809348 | Common:3; Rare:99 | ||||
| chr16:71845905-71846017 | Common:1; Rare:35 | ||||
| chr16:71895254-71895596 | Common:3; Rare:130 | ||||
| chr16:72008514-72008765 | Common:5; Rare:91; Clinvar (benign):1 | ||||
| chr16:72093579-72093934 | Rare:89 | ||||
| chr16:74296460-74296983 | Common:1; Rare:174 | ||||
| chr16:74304066-74304381 | Common:2; Rare:69 |