| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31010445-31010547 | Rare:19 | ||||
| chr16:31033460-31033821 | Common:1; Rare:104 | ||||
| chr16:31073716-31073848 | Rare:41 | ||||
| chr16:31074182-31074464 | Common:2; Rare:76 | ||||
| chr16:31074645-31074877 | Common:2; Rare:48 | ||||
| chr16:31093365-31093690 | Common:2; Rare:70; Clinvar (benign):1 | ||||
| chr16:31094536-31095013 | Common:1; Rare:153; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:31108209-31108506 | Common:1; Rare:60 | ||||
| chr16:31180592-31180821 | Common:3; Rare:82 | ||||
| chr16:31190755-31191180 | Common:1; Rare:139; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr16:31202284-31202343 | Common:1; Rare:17 | ||||
| chr16:31202627-31203006 | Common:2; Rare:125 | ||||
| chr16:31213716-31214051 | Common:1; Rare:48 | ||||
| chr16:31459324-31459517 | Common:1; Rare:79 | ||||
| chr16:31471978-31472186 | Rare:49 |