| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30355211-30355539 | Common:2; Rare:103 | ||||
| chr16:30762063-30762334 | Common:3; Rare:91 | ||||
| chr16:31471931-31472181 | Rare:55 | ||||
| chr16:31508389-31508478 | Common:1; Rare:34 | ||||
| chr16:46689137-46689366 | Common:1; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689466-46689708 | Common:2; Rare:90; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:47461032-47461343 | Common:2; Rare:110; Clinvar (benign):1 | ||||
| chr16:53703821-53704162 | Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:54286742-54286957 | Common:1; Rare:66 | ||||
| chr16:56451303-56451587 | Common:1; Rare:84 | ||||
| chr16:56608368-56608756 | Common:4; Rare:115 | ||||
| chr16:56625643-56625799 | Rare:44 | ||||
| chr16:56638533-56638669 | Rare:57 | ||||
| chr16:56730001-56730192 | Common:1; Rare:44 | ||||
| chr16:56931896-56932147 | Common:2; Rare:115 |