| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:203536962-203537308 | Rare:60 | ||||
| chr1:203538080-203538396 | Common:2; Rare:61 | ||||
| chr1:203551640-203551870 | Rare:38 | ||||
| chr1:203629546-203629722 | Rare:35 | ||||
| chr1:203629976-203630089 | Common:1; Rare:11 | ||||
| chr1:203650441-203650728 | Common:2; Rare:65 | ||||
| chr1:203693319-203693374 | Rare:4 | ||||
| chr1:203756638-203756778 | Rare:23 | ||||
| chr1:203860247-203860550 | Common:4; Rare:53 | ||||
| chr1:204074623-204074828 | Rare:34 | ||||
| chr1:204075257-204075281 | Rare:2 | ||||
| chr1:204080434-204080736 | Common:1; Rare:50 | ||||
| chr1:204104768-204104921 | Rare:37 | ||||
| chr1:204129157-204129250 | Rare:28 | ||||
| chr1:204190316-204190575 | Common:9; Rare:81; Clinvar (benign):1; Clinvar (pathogenic):1 |