| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48597171-48597275 | Rare:16 | ||||
| chr17:48610782-48611060 | Common:2; Rare:78 | ||||
| chr17:48841451-48841669 | Common:2; Rare:21 | ||||
| chr17:48908318-48908455 | Common:1; Rare:33 | ||||
| chr17:48944765-48944928 | Common:2; Rare:56 | ||||
| chr17:49210205-49210436 | Common:2; Rare:34 | ||||
| chr17:49210562-49210718 | Rare:23 | ||||
| chr17:49230768-49230812 | Rare:12 | ||||
| chr17:49414833-49415130 | Common:2; Rare:69 | ||||
| chr17:49646419-49646879 | Common:3; Rare:79 | ||||
| chr17:49707880-49707982 | Rare:54 | ||||
| chr17:49708148-49708344 | Common:1; Rare:60 | ||||
| chr17:49788567-49788789 | Common:1; Rare:74 | ||||
| chr17:50055872-50056133 | Common:4; Rare:64 | ||||
| chr17:50165864-50166041 | Common:2; Rare:53; Clinvar:3; Clinvar (benign):3 |