| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:57628396-57628730 | Common:4; Rare:79 | ||||
| chr16:57646768-57646960 | Common:3; Rare:30 | ||||
| chr16:57668190-57668325 | Common:1; Rare:28 | ||||
| chr16:57984906-57985252 | Common:5; Rare:112 | ||||
| chr16:57999590-57999626 | Rare:7 | ||||
| chr16:58000526-58000797 | Common:2; Rare:67 | ||||
| chr16:58001318-58001458 | Rare:41 | ||||
| chr16:58025675-58025751 | Rare:24 | ||||
| chr16:58129211-58129529 | Common:3; Rare:92 | ||||
| chr16:58515408-58515534 | Common:2; Rare:49 | ||||
| chr16:65121971-65122208 | Common:1; Rare:83 | ||||
| chr16:66366525-66366754 | Common:3; Rare:47 | ||||
| chr16:66549813-66550019 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:66552461-66552695 | Rare:100 | ||||
| chr16:66604033-66604276 | Common:6; Rare:60 |