| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19004707-19004882 | Common:1; Rare:55 | ||||
| chr17:19362565-19362773 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:19377622-19377793 | Common:2; Rare:44 | ||||
| chr17:19377875-19378033 | Common:1; Rare:43 | ||||
| chr17:19378116-19378537 | Common:2; Rare:103 | ||||
| chr17:19648007-19648182 | Rare:38 | ||||
| chr17:19648602-19649107 | Common:3; Rare:185; Clinvar (benign):1 | ||||
| chr17:19745698-19745910 | Common:3; Rare:34 | ||||
| chr17:19748258-19748692 | Common:3; Rare:104 | ||||
| chr17:19977778-19977962 | Common:1; Rare:63 | ||||
| chr17:20008669-20008870 | Common:1; Rare:47 | ||||
| chr17:20009086-20009412 | Common:3; Rare:88 | ||||
| chr17:20155700-20156085 | Common:1; Rare:111 | ||||
| chr17:21042234-21042394 | Common:1; Rare:66 | ||||
| chr17:21043390-21043511 | Common:1; Rare:48 |