| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41835414-41835814 | Common:5; Rare:75 | ||||
| chr17:41835973-41836483 | Common:7; Rare:287 | ||||
| chr17:41838038-41838438 | Common:2; Rare:83 | ||||
| chr17:41864757-41865166 | Rare:220 | ||||
| chr17:41865220-41865698 | Common:8; Rare:666 | ||||
| chr17:41918262-41918662 | Common:1; Rare:82 | ||||
| chr17:41918879-41919385 | Common:12; Rare:773; Clinvar:5 | ||||
| chr17:41930041-41930860 | Common:2; Rare:727; Clinvar (pathogenic):1 | ||||
| chr17:41965838-41966879 | Common:12; Rare:684 | ||||
| chr17:41967123-41967532 | Rare:134 | ||||
| chr17:41970451-41970851 | Common:3; Rare:77 | ||||
| chr17:42016352-42016483 | Rare:22 | ||||
| chr17:42016526-42017090 | Common:4; Rare:425 | ||||
| chr17:42017120-42018767 | Common:9; Rare:1426 | ||||
| chr17:42019852-42020254 | Common:5; Rare:415 |