| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42773375-42773484 | Rare:35 | ||||
| chr17:42833340-42833456 | Rare:43 | ||||
| chr17:42964437-42964534 | Rare:47 | ||||
| chr17:43125466-43125590 | Rare:19; Clinvar (benign):1 | ||||
| chr17:43170325-43170712 | Common:3; Rare:74 | ||||
| chr17:43171034-43171255 | Rare:69 | ||||
| chr17:44070581-44070911 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123599-44123840 | Common:3; Rare:68 | ||||
| chr17:44170530-44170737 | Rare:40 | ||||
| chr17:44186691-44187037 | Rare:111 | ||||
| chr17:44221236-44221390 | Rare:45 | ||||
| chr17:44324760-44324976 | Common:2; Rare:80 | ||||
| chr17:44350277-44350793 | Common:1; Rare:181; Clinvar:9; Clinvar (benign):6 | ||||
| chr17:44503367-44503662 | Rare:123 | ||||
| chr17:44899383-44899479 | Rare:42 |