| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5486801-5486933 | Common:4; Rare:40 | ||||
| chr17:6640646-6641070 | Common:7; Rare:126 | ||||
| chr17:6651553-6651720 | Common:1; Rare:63 | ||||
| chr17:7012315-7012686 | Rare:128 | ||||
| chr17:7219824-7219956 | Common:3; Rare:61; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7224008-7224345 | Rare:113; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):8 | ||||
| chr17:7224353-7224714 | Common:4; Rare:133; Clinvar:11; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr17:7224752-7224983 | Common:1; Rare:84; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr17:7242100-7242214 | Common:1; Rare:23 | ||||
| chr17:7242239-7242510 | Common:1; Rare:88 | ||||
| chr17:7251963-7252455 | Common:2; Rare:174 | ||||
| chr17:7281420-7281774 | Common:3; Rare:95 | ||||
| chr17:7307904-7308070 | Common:1; Rare:43 | ||||
| chr17:7315036-7315185 | Common:1; Rare:55 | ||||
| chr17:7350736-7350942 | Rare:49 |