| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:169367696-169368307 | Common:4; Rare:136 | ||||
| chr1:169368561-169368610 | Rare:10 | ||||
| chr1:169485674-169486234 | Common:2; Rare:161; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:169586470-169586530 | Rare:16 | ||||
| chr1:169711550-169711762 | Rare:58 | ||||
| chr1:169794649-169795189 | Common:5; Rare:127 | ||||
| chr1:169795835-169795880 | Common:1; Rare:12 | ||||
| chr1:169893500-169893811 | Common:4; Rare:100 | ||||
| chr1:169893812-169894044 | Common:2; Rare:67 | ||||
| chr1:169894250-169894403 | Common:2; Rare:50 | ||||
| chr1:170074423-170074786 | Common:3; Rare:113 | ||||
| chr1:170531739-170531874 | Rare:34 | ||||
| chr1:170531949-170532224 | Common:2; Rare:105; Clinvar:1 | ||||
| chr1:170532403-170532454 | Common:1; Rare:20 | ||||
| chr1:171313947-171314201 | Common:1; Rare:54 |