| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43778812-43779212 | Common:3; Rare:243 | ||||
| chr17:43832396-43833520 | Common:6; Rare:510 | ||||
| chr17:43900540-43900840 | Common:1; Rare:102 | ||||
| chr17:43907976-43908376 | Common:2; Rare:103 | ||||
| chr17:44014158-44015253 | Common:13; Rare:678 | ||||
| chr17:44066121-44067051 | Common:7; Rare:822 | ||||
| chr17:44067199-44068036 | Common:1; Rare:250 | ||||
| chr17:44069858-44070258 | Common:2; Rare:82 | ||||
| chr17:44070480-44071022 | Common:25; Rare:884; Clinvar:29; Clinvar (benign):14 | ||||
| chr17:44071001-44071913 | Common:3; Rare:459; Clinvar:7; Clinvar (pathogenic):9 | ||||
| chr17:44086720-44087270 | Common:12; Rare:529 | ||||
| chr17:44111105-44111651 | Common:1; Rare:388 | ||||
| chr17:44123510-44123918 | Common:21; Rare:519 | ||||
| chr17:44124009-44124116 | Common:2; Rare:55 | ||||
| chr17:44124076-44124476 | Common:1; Rare:87 |