| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2393768-2394100 | Common:3; Rare:130 | ||||
| chr17:2396775-2397113 | Common:2; Rare:83 | ||||
| chr17:2511512-2511674 | Rare:23 | ||||
| chr17:2511775-2512061 | Common:3; Rare:79 | ||||
| chr17:2593427-2593748 | Common:4; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:2593805-2594019 | Common:1; Rare:49; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:2594030-2594256 | Rare:69 | ||||
| chr17:2711218-2711349 | Common:2; Rare:36 | ||||
| chr17:2711677-2712075 | Common:2; Rare:107 | ||||
| chr17:3557742-3557957 | Common:4; Rare:46; Clinvar:4; Clinvar (benign):5 | ||||
| chr17:3636146-3636548 | Common:5; Rare:121; Clinvar (benign):2 | ||||
| chr17:3636677-3636795 | Common:1; Rare:34; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:3668413-3668927 | Common:3; Rare:201 | ||||
| chr17:3696040-3696195 | Rare:43 | ||||
| chr17:3723731-3724155 | Common:1; Rare:213 |