| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41812620-41812731 | Common:3; Rare:18 | ||||
| chr17:41835998-41836322 | Common:2; Rare:89 | ||||
| chr17:41930512-41930661 | Rare:41 | ||||
| chr17:41966610-41966885 | Common:1; Rare:99 | ||||
| chr17:42016543-42016637 | Rare:11 | ||||
| chr17:42017382-42017539 | Common:1; Rare:64 | ||||
| chr17:42017573-42017576 | Rare:1 | ||||
| chr17:42017577-42017687 | Rare:34 | ||||
| chr17:42121338-42121479 | Rare:36 | ||||
| chr17:42276260-42276582 | Rare:115 | ||||
| chr17:42287292-42287455 | Common:1; Rare:41 | ||||
| chr17:42289124-42289366 | Common:2; Rare:60 | ||||
| chr17:42316817-42317043 | Rare:49 | ||||
| chr17:42388585-42388887 | Common:1; Rare:75 | ||||
| chr17:42422720-42423399 | Common:2; Rare:227; Clinvar:6; Clinvar (pathogenic):1 |