| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7329310-7329826 | Common:11; Rare:245 | ||||
| chr17:7351586-7351850 | Rare:89 | ||||
| chr17:7351870-7352370 | Common:1; Rare:203 | ||||
| chr17:7403292-7403694 | Common:3; Rare:165 | ||||
| chr17:7404063-7404332 | Common:1; Rare:136 | ||||
| chr17:7440410-7440950 | Common:2; Rare:177 | ||||
| chr17:7479451-7479743 | Common:2; Rare:87 | ||||
| chr17:7484208-7484391 | Common:3; Rare:155 | ||||
| chr17:7484690-7484834 | Rare:119 | ||||
| chr17:7548610-7549177 | Common:4; Rare:153 | ||||
| chr17:7557780-7558410 | Common:5; Rare:195 | ||||
| chr17:7561803-7562020 | Common:4; Rare:114 | ||||
| chr17:7583735-7583868 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:7584057-7584361 | Common:1; Rare:90 | ||||
| chr17:7614681-7615400 | Rare:348 |