| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:6444174-6444481 | Common:2; Rare:98 | ||||
| chr17:6640646-6641097 | Common:7; Rare:141 | ||||
| chr17:6651574-6651727 | Common:1; Rare:49 | ||||
| chr17:7012317-7012686 | Rare:126 | ||||
| chr17:7224228-7224385 | Rare:50; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr17:7234364-7234668 | Common:2; Rare:139 | ||||
| chr17:7241766-7241916 | Common:2; Rare:31 | ||||
| chr17:7251963-7252310 | Common:1; Rare:136 | ||||
| chr17:7306704-7307061 | Common:1; Rare:95 | ||||
| chr17:7315084-7315435 | Common:4; Rare:125 | ||||
| chr17:7352035-7352220 | Rare:66 | ||||
| chr17:7438183-7438320 | Rare:31 | ||||
| chr17:7479496-7479753 | Common:1; Rare:45 | ||||
| chr17:7484234-7484391 | Common:2; Rare:70 | ||||
| chr17:7577056-7577425 | Common:1; Rare:91 |