| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41966579-41966837 | Common:2; Rare:88 | ||||
| chr17:42016543-42016809 | Common:1; Rare:48 | ||||
| chr17:42017364-42017487 | Rare:54 | ||||
| chr17:42017492-42017710 | Common:1; Rare:63 | ||||
| chr17:42112684-42112808 | Common:1; Rare:34 | ||||
| chr17:42117502-42117782 | Rare:78 | ||||
| chr17:42287160-42287442 | Common:1; Rare:54 | ||||
| chr17:42422609-42423283 | Common:1; Rare:247; Clinvar:7; Clinvar (pathogenic):2 | ||||
| chr17:42423307-42423316 | Rare:2 | ||||
| chr17:42566883-42567160 | Common:3; Rare:96 | ||||
| chr17:42577671-42577869 | Common:1; Rare:102 | ||||
| chr17:42609321-42609761 | Common:8; Rare:183; Clinvar (benign):2 | ||||
| chr17:42659362-42659475 | Rare:30 | ||||
| chr17:42761022-42761284 | Rare:76 | ||||
| chr17:42798637-42798770 | Rare:42 |