| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7352009-7352282 | Rare:88 | ||||
| chr17:7404037-7404322 | Common:1; Rare:97 | ||||
| chr17:7438146-7438320 | Common:1; Rare:37 | ||||
| chr17:7440761-7440810 | Rare:14 | ||||
| chr17:7479517-7479753 | Common:1; Rare:40 | ||||
| chr17:7484214-7484387 | Common:1; Rare:73 | ||||
| chr17:7484697-7484852 | Rare:61 | ||||
| chr17:7497854-7498145 | Common:3; Rare:116 | ||||
| chr17:7548997-7549222 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:7558233-7558331 | Rare:25 | ||||
| chr17:7558715-7559027 | Common:1; Rare:62 | ||||
| chr17:7561784-7562008 | Common:2; Rare:61 | ||||
| chr17:7577032-7577487 | Common:1; Rare:113 | ||||
| chr17:7583564-7583881 | Common:1; Rare:128; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7584056-7584122 | Rare:20 |