| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4833250-4833520 | Rare:72 | ||||
| chr17:4939892-4940365 | Common:2; Rare:139 | ||||
| chr17:4967774-4967866 | Rare:39 | ||||
| chr17:4987633-4987751 | Common:1; Rare:48 | ||||
| chr17:5078336-5078518 | Common:4; Rare:51 | ||||
| chr17:5191826-5192040 | Rare:69 | ||||
| chr17:5419628-5420208 | Common:6; Rare:184 | ||||
| chr17:5486158-5486419 | Common:4; Rare:109 | ||||
| chr17:5486796-5486920 | Common:4; Rare:37 | ||||
| chr17:6640657-6641077 | Common:7; Rare:129 | ||||
| chr17:6651574-6651747 | Common:1; Rare:53 | ||||
| chr17:7012317-7012718 | Rare:132 | ||||
| chr17:7022953-7023098 | Common:1; Rare:37 | ||||
| chr17:7219786-7219949 | Common:3; Rare:73; Clinvar:5; Clinvar (benign):1 | ||||
| chr17:7224318-7225060 | Common:5; Rare:270; Clinvar:23; Clinvar (benign):26; Clinvar (pathogenic):7 |