| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43546265-43546616 | Common:3; Rare:143 | ||||
| chr17:43778859-43779133 | Common:2; Rare:130 | ||||
| chr17:43833101-43833327 | Common:2; Rare:100 | ||||
| chr17:43900566-43900754 | Rare:112 | ||||
| chr17:44066110-44066490 | Common:1; Rare:104 | ||||
| chr17:44070599-44071132 | Common:6; Rare:300; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr17:44123571-44123889 | Common:6; Rare:169 | ||||
| chr17:44123930-44124180 | Common:2; Rare:102 | ||||
| chr17:44141680-44142108 | Common:3; Rare:184 | ||||
| chr17:44186588-44187051 | Common:4; Rare:307 | ||||
| chr17:44187142-44187301 | Rare:80 | ||||
| chr17:44198320-44198830 | Common:4; Rare:179 | ||||
| chr17:44199225-44199625 | Common:4; Rare:232 | ||||
| chr17:44199867-44200440 | Common:6; Rare:419 | ||||
| chr17:44218436-44218809 | Common:1; Rare:218 |