| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:49707884-49708208 | Rare:142 | ||||
| chr17:49788470-49788750 | Common:1; Rare:92 | ||||
| chr17:50186315-50186685 | Common:2; Rare:95; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:50188740-50189011 | Rare:72; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50189203-50189683 | Rare:107; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:50192825-50193039 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:50373146-50373246 | Common:3; Rare:46 | ||||
| chr17:50719482-50719768 | Rare:105 | ||||
| chr17:51166676-51166951 | Rare:78 | ||||
| chr17:51260301-51260593 | Common:3; Rare:120 | ||||
| chr17:54968608-54968799 | Common:3; Rare:91 | ||||
| chr17:56833804-56834139 | Common:3; Rare:91 | ||||
| chr17:56913960-56914175 | Common:1; Rare:60 | ||||
| chr17:57084986-57085095 | Rare:38 | ||||
| chr17:57849973-57850274 | Common:1; Rare:102 |