| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4143004-4143264 | Rare:83 | ||||
| chr17:4143597-4143740 | Common:4; Rare:80 | ||||
| chr17:4263937-4264099 | Rare:65 | ||||
| chr17:4555320-4555515 | Common:3; Rare:91 | ||||
| chr17:4704093-4704271 | Rare:86 | ||||
| chr17:4731295-4731507 | Common:2; Rare:68 | ||||
| chr17:4739374-4739448 | Common:2; Rare:26 | ||||
| chr17:4739464-4739929 | Common:6; Rare:104 | ||||
| chr17:4806994-4807210 | Common:4; Rare:67 | ||||
| chr17:4833173-4833608 | Common:1; Rare:115 | ||||
| chr17:4899383-4899494 | Common:1; Rare:71; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:4939907-4940025 | Rare:42 | ||||
| chr17:4940034-4940390 | Common:2; Rare:96 | ||||
| chr17:4947952-4948005 | Rare:14 | ||||
| chr17:4948133-4948240 | Rare:37 |