| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:219173796-219173896 | Common:1; Rare:54 | ||||
| chr1:221742081-221742325 | Common:1; Rare:71 | ||||
| chr1:222617879-222618117 | Common:3; Rare:61 | ||||
| chr1:222644070-222644412 | Common:3; Rare:102 | ||||
| chr1:222712434-222712888 | Common:3; Rare:154 | ||||
| chr1:222713243-222713405 | Common:1; Rare:49 | ||||
| chr1:224434792-224434969 | Rare:48 | ||||
| chr1:225428005-225428286 | Common:3; Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
| chr1:225777716-225777949 | Common:3; Rare:81 | ||||
| chr1:225999305-225999617 | Common:2; Rare:107 | ||||
| chr1:226062000-226062094 | Common:1; Rare:31 | ||||
| chr1:226186425-226186756 | Common:1; Rare:90 | ||||
| chr1:226870493-226870640 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr1:226939985-226940435 | Common:1; Rare:149; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:226982680-226983041 | Common:3; Rare:138; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):6 |