| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:73164880-73165028 | Common:2; Rare:45 | ||||
| chr17:73192762-73193076 | Common:15; Rare:125; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73205942-73205973 | Common:1; Rare:6 | ||||
| chr17:73232120-73232736 | Common:4; Rare:239 | ||||
| chr17:73644268-73644561 | Common:1; Rare:71 | ||||
| chr17:74203405-74203806 | Common:3; Rare:115 | ||||
| chr17:74213345-74213571 | Common:4; Rare:51 | ||||
| chr17:74431883-74432301 | Common:1; Rare:150 | ||||
| chr17:74432409-74432504 | Rare:21 | ||||
| chr17:74737109-74737263 | Rare:57 | ||||
| chr17:74748746-74749120 | Common:4; Rare:133; Clinvar:2 | ||||
| chr17:74749140-74749281 | Common:1; Rare:44; Clinvar:1 | ||||
| chr17:74776031-74776565 | Common:5; Rare:150 | ||||
| chr17:74972652-74972874 | Common:2; Rare:62 | ||||
| chr17:74987537-74987633 | Rare:28 |