| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7012255-7012710 | Rare:146 | ||||
| chr17:7013127-7013430 | Common:1; Rare:80 | ||||
| chr17:7014242-7014370 | Rare:36 | ||||
| chr17:7014488-7014831 | Common:7; Rare:113 | ||||
| chr17:7015054-7015188 | Common:1; Rare:42 | ||||
| chr17:7015221-7015513 | Common:1; Rare:55 | ||||
| chr17:7015613-7015941 | Common:3; Rare:95 | ||||
| chr17:7035698-7036220 | Common:3; Rare:118 | ||||
| chr17:7204828-7205083 | Rare:56 | ||||
| chr17:7219783-7219991 | Common:3; Rare:89; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:7234356-7234692 | Common:2; Rare:153 | ||||
| chr17:7237660-7238036 | Common:1; Rare:104 | ||||
| chr17:7238245-7238374 | Rare:13 | ||||
| chr17:7239362-7239485 | Rare:33 | ||||
| chr17:7242421-7242544 | Rare:43 |