| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127117546-127117694 | Rare:31 | ||||
| chr6:128055730-128056015 | Common:4; Rare:43 | ||||
| chr6:128949031-128949145 | Rare:29 | ||||
| chr6:129353986-129354070 | Rare:9 | ||||
| chr6:129403691-129403903 | Common:6; Rare:55; Clinvar:1; Clinvar (benign):3 | ||||
| chr6:129427541-129427782 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr6:129438424-129438725 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):4 | ||||
| chr6:129452849-129453132 | Rare:80; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:129453967-129454285 | Rare:79; Clinvar:5; Clinvar (benign):4 | ||||
| chr6:129459952-129460306 | Common:1; Rare:86; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr6:129464927-129465254 | Common:1; Rare:72; Clinvar:1 | ||||
| chr6:129472935-129473259 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:129478502-129478808 | Common:1; Rare:93; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr6:129481036-129481430 | Common:1; Rare:97; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr6:129489516-129489730 | Common:1; Rare:23 |