| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:19525249-19525309 | Common:1; Rare:13 | ||||
| chr16:19717178-19717506 | Common:1; Rare:68 | ||||
| chr16:20216894-20217131 | Common:2; Rare:45 | ||||
| chr16:20747258-20747502 | Common:1; Rare:37 | ||||
| chr16:21116304-21116440 | Rare:26 | ||||
| chr16:21261057-21261310 | Common:2; Rare:47; Clinvar (benign):1 | ||||
| chr16:21263740-21264014 | Common:1; Rare:46 | ||||
| chr16:21300685-21300950 | Common:3; Rare:49 | ||||
| chr16:21301308-21301980 | Common:8; Rare:205 | ||||
| chr16:21356502-21356643 | Rare:32 | ||||
| chr16:21358393-21358546 | Common:1; Rare:43 | ||||
| chr16:21360326-21360382 | Rare:13 | ||||
| chr16:21360397-21360458 | Rare:14 | ||||
| chr16:21363997-21364046 | Common:1; Rare:10 | ||||
| chr16:21365733-21365773 | Rare:9 |