| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7352430-7352449 | Rare:2 | ||||
| chr17:7394177-7394274 | Rare:17 | ||||
| chr17:7394472-7394823 | Common:3; Rare:97 | ||||
| chr17:7394842-7395108 | Rare:43 | ||||
| chr17:7403314-7403647 | Common:1; Rare:73 | ||||
| chr17:7403746-7403917 | Common:5; Rare:46 | ||||
| chr17:7404046-7404366 | Common:1; Rare:99 | ||||
| chr17:7404553-7404703 | Common:2; Rare:49 | ||||
| chr17:7404732-7404932 | Common:4; Rare:49 | ||||
| chr17:7440904-7441043 | Common:2; Rare:26 | ||||
| chr17:7445393-7445517 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr17:7455366-7455687 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:7455775-7455875 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7455936-7456158 | Common:5; Rare:50; Clinvar (benign):1 | ||||
| chr17:7479024-7479178 | Rare:41 |