| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3636241-3636479 | Common:4; Rare:63; Clinvar (benign):1 | ||||
| chr17:3668547-3668826 | Common:2; Rare:109 | ||||
| chr17:3723797-3723907 | Common:1; Rare:59 | ||||
| chr17:3892955-3893257 | Common:3; Rare:101 | ||||
| chr17:4142970-4143225 | Common:3; Rare:90 | ||||
| chr17:4143609-4143740 | Common:4; Rare:74 | ||||
| chr17:4263937-4264042 | Rare:46 | ||||
| chr17:4555304-4555518 | Common:3; Rare:99 | ||||
| chr17:4704110-4704231 | Rare:69 | ||||
| chr17:4731293-4731475 | Common:2; Rare:53 | ||||
| chr17:4739537-4739670 | Rare:35 | ||||
| chr17:4807008-4807192 | Common:4; Rare:62 | ||||
| chr17:4899384-4899475 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:4939916-4940348 | Common:2; Rare:127 | ||||
| chr17:4948502-4948732 | Common:2; Rare:82 |