| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44915194-44915479 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr17:44915482-44915664 | Rare:41; Clinvar (benign):1 | ||||
| chr17:45060987-45061339 | Common:2; Rare:93 | ||||
| chr17:45132364-45132631 | Common:1; Rare:83 | ||||
| chr17:45148152-45148598 | Common:1; Rare:152 | ||||
| chr17:45161494-45161838 | Common:1; Rare:90 | ||||
| chr17:45490708-45490888 | Rare:61 | ||||
| chr17:45620198-45620362 | Rare:40 | ||||
| chr17:45894218-45894684 | Common:5; Rare:137; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:46192872-46193019 | Common:1; Rare:41 | ||||
| chr17:46225349-46225477 | Common:1; Rare:32 | ||||
| chr17:46579669-46579990 | Rare:31 | ||||
| chr17:46922827-46923187 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189231-47189582 | Rare:87 | ||||
| chr17:47323687-47324028 | Common:4; Rare:117 |