| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2303461-2303626 | Rare:63 | ||||
| chr17:2303722-2303987 | Common:2; Rare:101 | ||||
| chr17:2336423-2336550 | Rare:50 | ||||
| chr17:2375971-2376182 | Common:1; Rare:69 | ||||
| chr17:2511778-2512017 | Common:2; Rare:71 | ||||
| chr17:2593491-2593658 | Common:2; Rare:61 | ||||
| chr17:2593857-2593993 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:2594163-2594191 | Rare:7 | ||||
| chr17:2711733-2712031 | Common:2; Rare:84 | ||||
| chr17:2796205-2796472 | Common:1; Rare:60 | ||||
| chr17:3636121-3636527 | Common:4; Rare:130; Clinvar (benign):1 | ||||
| chr17:3636690-3636772 | Common:1; Rare:22; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3668515-3668820 | Common:3; Rare:123 | ||||
| chr17:3723736-3723938 | Common:1; Rare:112 | ||||
| chr17:3892952-3893194 | Common:3; Rare:77 |