| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:186375093-186375974 | Common:3; Rare:637 | ||||
| chr1:186680020-186680660 | Common:5; Rare:155 | ||||
| chr1:190474727-190474909 | Common:2; Rare:38 | ||||
| chr1:190477506-190478250 | Common:2; Rare:217 | ||||
| chr1:190478359-190479039 | Common:15; Rare:223 | ||||
| chr1:192808832-192809085 | Common:7; Rare:166 | ||||
| chr1:193059237-193059741 | Common:1; Rare:613 | ||||
| chr1:193105295-193105771 | Common:10; Rare:420 | ||||
| chr1:193121613-193122234 | Common:8; Rare:566; Clinvar:15; Clinvar (benign):13; Clinvar (pathogenic):3 | ||||
| chr1:196608730-196609060 | Common:1; Rare:63 | ||||
| chr1:197146505-197146918 | Common:1; Rare:241; Clinvar:10; Clinvar (benign):1 | ||||
| chr1:197200452-197200852 | Common:6; Rare:142 | ||||
| chr1:197774740-197775140 | Common:4; Rare:149 | ||||
| chr1:197775157-197776250 | Common:6; Rare:401 | ||||
| chr1:197902481-197902727 | Common:2; Rare:156 |