| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219245423-219245531 | Rare:33 | ||||
| chr2:219253859-219254056 | Common:1; Rare:62 | ||||
| chr2:219279207-219279540 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr2:219418580-219419039 | Common:2; Rare:149; Clinvar:33; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr2:219420372-219420656 | Common:2; Rare:76; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr2:219460569-219460867 | Common:3; Rare:65 | ||||
| chr2:219498496-219498935 | Common:3; Rare:94 | ||||
| chr2:219597751-219597909 | Common:1; Rare:64 | ||||
| chr2:221572275-221572448 | Common:2; Rare:61 | ||||
| chr2:222424438-222424564 | Rare:42 | ||||
| chr2:222656013-222656446 | Common:3; Rare:144 | ||||
| chr2:223052086-223052191 | Rare:22 | ||||
| chr2:223957301-223957472 | Common:3; Rare:67 | ||||
| chr2:226835786-226836136 | Common:1; Rare:137 | ||||
| chr2:226836373-226836419 | Common:1; Rare:10 |