| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:169107807-169107977 | Common:1; Rare:35 | ||||
| chr1:169108403-169108485 | Common:1; Rare:13 | ||||
| chr1:169367249-169367345 | Common:1; Rare:18 | ||||
| chr1:169367682-169368062 | Common:2; Rare:92 | ||||
| chr1:169368147-169368361 | Common:2; Rare:40 | ||||
| chr1:169368579-169368675 | Common:1; Rare:17 | ||||
| chr1:169485245-169485457 | Rare:44 | ||||
| chr1:169485505-169486426 | Common:5; Rare:257; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:169794511-169794753 | Common:2; Rare:48 | ||||
| chr1:169794810-169795243 | Common:3; Rare:112 | ||||
| chr1:169893376-169893536 | Common:1; Rare:29 | ||||
| chr1:169893538-169893820 | Common:4; Rare:94 | ||||
| chr1:169893867-169894037 | Common:2; Rare:51 | ||||
| chr1:169894257-169894430 | Common:2; Rare:56 | ||||
| chr1:170074172-170074213 | Rare:13 |