| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:54286369-54286431 | Common:1; Rare:9 | ||||
| chr16:54286568-54287017 | Common:3; Rare:122 | ||||
| chr16:54930550-54930760 | Common:1; Rare:54 | ||||
| chr16:55479447-55479494 | Rare:20; Clinvar:2 | ||||
| chr16:55566616-55567217 | Common:1; Rare:168 | ||||
| chr16:56336303-56336523 | Common:1; Rare:52 | ||||
| chr16:56451306-56451605 | Common:1; Rare:98 | ||||
| chr16:56505961-56506137 | Common:1; Rare:38; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:56519749-56520127 | Common:6; Rare:154; Clinvar:12; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr16:56608253-56608714 | Common:4; Rare:130 | ||||
| chr16:56625642-56625849 | Rare:63 | ||||
| chr16:56632202-56632494 | Common:1; Rare:82 | ||||
| chr16:56638533-56638716 | Rare:77 | ||||
| chr16:56657859-56658047 | Common:2; Rare:54 | ||||
| chr16:56667999-56668180 | Common:4; Rare:60 |