| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7043911-7044114 | Common:3; Rare:40 | ||||
| chr17:7219784-7219981 | Common:3; Rare:86; Clinvar:6; Clinvar (benign):2 | ||||
| chr17:7221295-7221675 | Common:9; Rare:122; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chr17:7221894-7221977 | Common:2; Rare:24; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr17:7234445-7234720 | Common:2; Rare:127 | ||||
| chr17:7241434-7241654 | Rare:47 | ||||
| chr17:7241787-7241930 | Common:2; Rare:32 | ||||
| chr17:7242209-7242490 | Common:1; Rare:91 | ||||
| chr17:7251940-7252078 | Common:1; Rare:58 | ||||
| chr17:7308810-7308986 | Rare:44 | ||||
| chr17:7313411-7313597 | Common:1; Rare:83 | ||||
| chr17:7315036-7315438 | Common:4; Rare:143 | ||||
| chr17:7350907-7350942 | Rare:6 | ||||
| chr17:7351626-7351743 | Rare:20 | ||||
| chr17:7352037-7352282 | Rare:82 |