| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:57803270-57803890 | Common:4; Rare:139 | ||||
| chr16:57862759-57863260 | Common:1; Rare:142 | ||||
| chr16:58000589-58000808 | Common:3; Rare:103 | ||||
| chr16:58001304-58001511 | Rare:130 | ||||
| chr16:58024760-58025150 | Rare:148 | ||||
| chr16:58025433-58025827 | Rare:244 | ||||
| chr16:58129264-58129583 | Common:6; Rare:182 | ||||
| chr16:58392808-58392924 | Common:1; Rare:26 | ||||
| chr16:58515353-58515538 | Common:6; Rare:119 | ||||
| chr16:58629698-58630179 | Common:5; Rare:220 | ||||
| chr16:58684694-58684811 | Rare:71 | ||||
| chr16:58734172-58734463 | Common:9; Rare:135 | ||||
| chr16:66427205-66427326 | Rare:45 | ||||
| chr16:66516760-66517450 | Common:2; Rare:227; Clinvar (benign):4; Clinvar (pathogenic):10 | ||||
| chr16:66549807-66549964 | Rare:109; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |