| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47941378-47941716 | Rare:94; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48047764-48047907 | Common:1; Rare:32 | ||||
| chr17:48048051-48048372 | Rare:86 | ||||
| chr17:48048599-48048829 | Common:4; Rare:34 | ||||
| chr17:48544437-48544658 | Common:1; Rare:90 | ||||
| chr17:48544713-48544770 | Common:2; Rare:18 | ||||
| chr17:48590239-48590435 | Common:1; Rare:43 | ||||
| chr17:48892341-48892543 | Common:9; Rare:64 | ||||
| chr17:48944758-48944894 | Common:1; Rare:49 | ||||
| chr17:49210582-49210712 | Rare:19 | ||||
| chr17:49788570-49788701 | Rare:36 | ||||
| chr17:50055697-50056161 | Common:6; Rare:99 | ||||
| chr17:50186889-50187115 | Common:1; Rare:68; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50191787-50192023 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:50192476-50192829 | Common:3; Rare:97; Clinvar:4; Clinvar (benign):9 |