| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43170254-43170718 | Common:3; Rare:97 | ||||
| chr17:43171003-43171294 | Common:1; Rare:102 | ||||
| chr17:43398881-43398996 | Common:1; Rare:33 | ||||
| chr17:43483657-43484074 | Rare:120 | ||||
| chr17:43778928-43779087 | Common:1; Rare:40 | ||||
| chr17:43833114-43833284 | Common:1; Rare:49 | ||||
| chr17:43900569-43900766 | Rare:69 | ||||
| chr17:43942437-43942599 | Rare:29 | ||||
| chr17:43953914-43954071 | Common:1; Rare:32 | ||||
| chr17:44066252-44066348 | Rare:34 | ||||
| chr17:44070562-44070986 | Common:3; Rare:141; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123506-44123889 | Common:3; Rare:113 | ||||
| chr17:44141780-44142062 | Common:1; Rare:70 | ||||
| chr17:44186623-44187274 | Common:1; Rare:204 | ||||
| chr17:44210439-44210691 | Rare:98 |