| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43398881-43398993 | Common:1; Rare:30 | ||||
| chr17:43778938-43779048 | Rare:23 | ||||
| chr17:44070612-44070947 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123599-44123840 | Common:3; Rare:68 | ||||
| chr17:44141703-44141956 | Common:1; Rare:52 | ||||
| chr17:44186673-44186998 | Common:1; Rare:115 | ||||
| chr17:44503369-44503727 | Rare:137 | ||||
| chr17:44899375-44899735 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:44947748-44947903 | Common:1; Rare:44 | ||||
| chr17:45060987-45061329 | Common:2; Rare:90 | ||||
| chr17:45148159-45148612 | Common:1; Rare:156 | ||||
| chr17:45160981-45161095 | Rare:28 | ||||
| chr17:46922844-46923181 | Common:3; Rare:92; Clinvar (benign):6 | ||||
| chr17:47649610-47649931 | Common:1; Rare:118 | ||||
| chr17:47970783-47971092 | Common:4; Rare:62 |