| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41688474-41689009 | Common:3; Rare:193 | ||||
| chr17:41689150-41689647 | Common:5; Rare:181 | ||||
| chr17:41689750-41689893 | Rare:33 | ||||
| chr17:41734513-41734697 | Common:4; Rare:109 | ||||
| chr17:41785217-41785409 | Common:1; Rare:41 | ||||
| chr17:41785945-41786304 | Common:2; Rare:77 | ||||
| chr17:41786345-41786470 | Common:1; Rare:18 | ||||
| chr17:41786590-41786750 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:41811477-41811569 | Rare:35 | ||||
| chr17:41811610-41811853 | Rare:72 | ||||
| chr17:41811871-41812330 | Rare:141 | ||||
| chr17:41812335-41812513 | Common:1; Rare:47 | ||||
| chr17:41812574-41812766 | Common:3; Rare:37; Clinvar:1 | ||||
| chr17:41812888-41813043 | Rare:44 | ||||
| chr17:41835414-41835697 | Common:4; Rare:52 |