| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27268719-27268872 | Common:1; Rare:52 | ||||
| chr16:27549865-27550167 | Common:2; Rare:118 | ||||
| chr16:28846265-28846623 | Common:2; Rare:123; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:28878341-28878584 | Common:2; Rare:59 | ||||
| chr16:28879744-28880072 | Common:3; Rare:85 | ||||
| chr16:28887715-28887928 | Rare:63 | ||||
| chr16:28902866-28903087 | Rare:84; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr16:29961994-29962130 | Common:1; Rare:38 | ||||
| chr16:29995610-29995713 | Rare:47 | ||||
| chr16:29996070-29996274 | Common:2; Rare:73 | ||||
| chr16:30064093-30064353 | Rare:53 | ||||
| chr16:30065579-30065857 | Rare:92 | ||||
| chr16:30069659-30069917 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):6 | ||||
| chr16:30075889-30076045 | Rare:51 | ||||
| chr16:30355210-30355437 | Common:1; Rare:80 |