| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42998582-42998811 | Rare:53 | ||||
| chr17:43125275-43125722 | Rare:121; Clinvar:7; Clinvar (benign):8 | ||||
| chr17:43170186-43170534 | Common:2; Rare:79 | ||||
| chr17:43170992-43171306 | Common:1; Rare:107 | ||||
| chr17:43211758-43211903 | Common:1; Rare:32 | ||||
| chr17:43491225-43491478 | Rare:49 | ||||
| chr17:43545862-43546225 | Common:2; Rare:60 | ||||
| chr17:43833086-43833432 | Common:2; Rare:89 | ||||
| chr17:43907517-43907618 | Rare:36 | ||||
| chr17:44066129-44066364 | Common:1; Rare:65 | ||||
| chr17:44070636-44070982 | Common:3; Rare:122; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123602-44123872 | Common:3; Rare:77 | ||||
| chr17:44186643-44187329 | Common:2; Rare:210 | ||||
| chr17:44188751-44189059 | Common:3; Rare:77 | ||||
| chr17:44212904-44213243 | Common:1; Rare:68 |