| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44070517-44070986 | Common:3; Rare:146; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44111143-44111453 | Rare:94 | ||||
| chr17:44123570-44123856 | Common:3; Rare:83 | ||||
| chr17:44123913-44124101 | Rare:41 | ||||
| chr17:44141764-44142090 | Common:1; Rare:79 | ||||
| chr17:44142370-44142612 | Common:2; Rare:60 | ||||
| chr17:44186498-44187052 | Common:3; Rare:173 | ||||
| chr17:44187153-44187304 | Rare:37 | ||||
| chr17:44198357-44198675 | Common:2; Rare:78 | ||||
| chr17:44199331-44199540 | Common:1; Rare:59 | ||||
| chr17:44199859-44200033 | Common:1; Rare:58 | ||||
| chr17:44200069-44200679 | Common:3; Rare:228 | ||||
| chr17:44210391-44210597 | Rare:94 | ||||
| chr17:44218406-44218916 | Common:1; Rare:156 | ||||
| chr17:44219174-44219377 | Common:2; Rare:69 |