| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43778297-43778440 | Rare:27 | ||||
| chr17:43778908-43779100 | Common:1; Rare:50 | ||||
| chr17:43780303-43780486 | Rare:31 | ||||
| chr17:43833101-43833294 | Common:1; Rare:55 | ||||
| chr17:43900576-43900745 | Rare:56 | ||||
| chr17:43907490-43907582 | Rare:30 | ||||
| chr17:44066294-44066339 | Rare:16 | ||||
| chr17:44070636-44070947 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44093428-44093615 | Common:1; Rare:68 | ||||
| chr17:44141809-44142042 | Common:1; Rare:64 | ||||
| chr17:44186604-44187050 | Common:2; Rare:155 | ||||
| chr17:44187161-44187301 | Rare:37 | ||||
| chr17:44220825-44221051 | Rare:73 | ||||
| chr17:44221232-44221413 | Rare:52 | ||||
| chr17:44222103-44222275 | Rare:36 |