| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43778925-43779078 | Rare:33 | ||||
| chr17:44070619-44070947 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44186651-44187002 | Common:1; Rare:128 | ||||
| chr17:44221211-44221356 | Rare:43 | ||||
| chr17:44308432-44308646 | Common:1; Rare:64 | ||||
| chr17:44324778-44324966 | Common:2; Rare:67 | ||||
| chr17:44345058-44345321 | Rare:55; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44503377-44503714 | Rare:132 | ||||
| chr17:44899375-44899741 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:44915298-44915485 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:44915487-44915646 | Rare:38; Clinvar (benign):1 | ||||
| chr17:45051571-45051692 | Rare:42 | ||||
| chr17:45060958-45061332 | Common:3; Rare:96 | ||||
| chr17:45148147-45148478 | Common:1; Rare:94 | ||||
| chr17:45161494-45161911 | Common:1; Rare:109 |