| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:38428167-38428488 | Common:9; Rare:112 | ||||
| chr17:38705005-38705334 | Common:2; Rare:78 | ||||
| chr17:38749818-38749870 | Rare:11 | ||||
| chr17:38825270-38825408 | Common:2; Rare:41 | ||||
| chr17:38869910-38870209 | Common:2; Rare:87 | ||||
| chr17:39200466-39200477 | Rare:2 | ||||
| chr17:39401614-39401792 | Common:1; Rare:49 | ||||
| chr17:39461363-39461519 | Common:1; Rare:42 | ||||
| chr17:39636809-39637182 | Common:3; Rare:106 | ||||
| chr17:39664905-39665467 | Common:4; Rare:137; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr17:39667663-39667972 | Common:1; Rare:51 | ||||
| chr17:39687980-39688164 | Rare:59 | ||||
| chr17:39927492-39927745 | Common:2; Rare:74 | ||||
| chr17:40054378-40054577 | Common:2; Rare:43 | ||||
| chr17:40121821-40122007 | Common:2; Rare:70 |