| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:58129243-58129581 | Common:4; Rare:106 | ||||
| chr16:58392813-58392889 | Common:1; Rare:21 | ||||
| chr16:58501348-58501537 | Rare:47 | ||||
| chr16:58515398-58515534 | Common:2; Rare:52 | ||||
| chr16:58629728-58629910 | Rare:55 | ||||
| chr16:58684704-58684840 | Rare:40 | ||||
| chr16:65122014-65122316 | Common:1; Rare:88 | ||||
| chr16:66549778-66549961 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:66552466-66552636 | Rare:76 | ||||
| chr16:66604538-66604721 | Rare:55 | ||||
| chr16:66925530-66925697 | Common:1; Rare:31 | ||||
| chr16:66934327-66934534 | Common:1; Rare:85 | ||||
| chr16:67028983-67029335 | Common:4; Rare:112 | ||||
| chr16:67109770-67109999 | Rare:78 | ||||
| chr16:67170420-67170555 | Common:1; Rare:23 |