| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42388392-42388823 | Common:1; Rare:119; Clinvar:3 | ||||
| chr17:42423209-42423496 | Common:1; Rare:77; Clinvar:1 | ||||
| chr17:42458730-42458914 | Common:1; Rare:71 | ||||
| chr17:42566887-42567116 | Common:3; Rare:79 | ||||
| chr17:42577651-42577825 | Rare:79 | ||||
| chr17:42609333-42609730 | Common:8; Rare:164; Clinvar (benign):2 | ||||
| chr17:42745023-42745114 | Common:2; Rare:30 | ||||
| chr17:42773358-42773475 | Rare:33 | ||||
| chr17:42833378-42833487 | Rare:44 | ||||
| chr17:42964422-42964543 | Rare:56 | ||||
| chr17:43125313-43125642 | Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170303-43170397 | Rare:16 | ||||
| chr17:43171000-43171249 | Rare:80 | ||||
| chr17:43398897-43398996 | Rare:26 | ||||
| chr17:43483657-43484034 | Rare:103 |