| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1073585-1073817 | Common:3; Rare:45 | ||||
| chr16:2673383-2673686 | Common:8; Rare:103 | ||||
| chr16:3021481-3021596 | Rare:45 | ||||
| chr16:4505322-4505607 | Rare:69 | ||||
| chr16:4797935-4798172 | Rare:134; Clinvar:12; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:29139564-29139668 | Common:2; Rare:19 | ||||
| chr16:29982885-29983143 | Common:1; Rare:88 | ||||
| chr16:30118058-30118386 | Common:2; Rare:82 | ||||
| chr16:30634282-30634553 | Common:1; Rare:70 | ||||
| chr16:30875333-30875465 | Rare:43 | ||||
| chr16:46757461-46757891 | Common:1; Rare:73 | ||||
| chr16:55324404-55324799 | Common:4; Rare:91 | ||||
| chr16:55330710-55330880 | Common:1; Rare:36 | ||||
| chr16:56617392-56617565 | Common:3; Rare:34 | ||||
| chr16:58438391-58438473 | Common:2; Rare:17 |