| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27549861-27550167 | Common:2; Rare:119 | ||||
| chr16:28491938-28492132 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:28553836-28554027 | Common:3; Rare:57 | ||||
| chr16:28554179-28554325 | Common:2; Rare:50 | ||||
| chr16:28623170-28623470 | Rare:108 | ||||
| chr16:28822534-28822749 | Common:1; Rare:77 | ||||
| chr16:28824319-28824517 | Common:2; Rare:73 | ||||
| chr16:28846250-28846696 | Common:2; Rare:150; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:28863733-28864001 | Common:3; Rare:65 | ||||
| chr16:28879883-28880058 | Common:3; Rare:52 | ||||
| chr16:28925159-28925370 | Rare:65 | ||||
| chr16:28974647-28974792 | Common:1; Rare:60 | ||||
| chr16:29454153-29454626 | |||||
| chr16:29790454-29790796 | Common:2; Rare:129; Clinvar (benign):2 | ||||
| chr16:29805494-29805641 | Common:1; Rare:66 |