| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31834552-31834895 | Common:2; Rare:79 | ||||
| chr6:31870687-31870825 | Common:2; Rare:40 | ||||
| chr6:31897646-31897791 | Rare:29 | ||||
| chr6:31945875-31946131 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr6:31958881-31959214 | Rare:111; Clinvar:8 | ||||
| chr6:31971735-31971908 | Common:1; Rare:25 | ||||
| chr6:31972454-31972660 | Common:1; Rare:76 | ||||
| chr6:32038257-32038494 | Common:4; Rare:62; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:32038497-32038821 | Common:5; Rare:93; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:32045769-32046144 | Common:2; Rare:66 | ||||
| chr6:32130205-32130393 | Common:1; Rare:35 | ||||
| chr6:32153486-32153598 | Rare:18 | ||||
| chr6:32153736-32154205 | Common:4; Rare:78 | ||||
| chr6:32154749-32155053 | Rare:60 | ||||
| chr6:32176054-32176248 | Common:1; Rare:39 |