| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:192808867-192809076 | Common:3; Rare:94 | ||||
| chr1:193059298-193059737 | Common:1; Rare:209 | ||||
| chr1:193060057-193060164 | Rare:35 | ||||
| chr1:193104961-193105152 | Rare:39 | ||||
| chr1:193105318-193105697 | Common:4; Rare:157 | ||||
| chr1:193121672-193122265 | Common:3; Rare:208; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr1:197146594-197146887 | Rare:86; Clinvar:3 | ||||
| chr1:197775018-197775168 | Rare:51 | ||||
| chr1:197775170-197775350 | Common:1; Rare:46 | ||||
| chr1:197775418-197775572 | Rare:42 | ||||
| chr1:197775620-197775840 | Common:2; Rare:45 | ||||
| chr1:197902508-197902674 | Common:1; Rare:55 | ||||
| chr1:197902858-197903033 | Common:2; Rare:91 | ||||
| chr1:198156915-198157087 | Common:1; Rare:68 | ||||
| chr1:198157559-198157752 | Common:1; Rare:69 |