| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7224872-7225070 | Common:1; Rare:75; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr17:7238570-7238694 | Common:2; Rare:7 | ||||
| chr17:7242240-7242587 | Common:1; Rare:110 | ||||
| chr17:7251689-7251770 | Common:1; Rare:24 | ||||
| chr17:7251916-7252438 | Common:3; Rare:181 | ||||
| chr17:7252474-7252927 | Common:3; Rare:178 | ||||
| chr17:7307406-7308125 | Common:5; Rare:192 | ||||
| chr17:7315036-7315435 | Common:4; Rare:142 | ||||
| chr17:7352035-7352240 | Rare:72 | ||||
| chr17:7403739-7404033 | Common:6; Rare:84 | ||||
| chr17:7479485-7479723 | Common:1; Rare:40 | ||||
| chr17:7484190-7484372 | Common:1; Rare:73 | ||||
| chr17:7484672-7484837 | Rare:69 | ||||
| chr17:7501372-7501617 | Rare:68 | ||||
| chr17:7511879-7512142 | Rare:66 |