| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79537399-79537672 | Rare:82; Clinvar:1 | ||||
| chr6:79631189-79631304 | Common:1; Rare:26 | ||||
| chr6:79947497-79947671 | Common:1; Rare:75; Clinvar:8; Clinvar (benign):2 | ||||
| chr6:80004452-80004716 | Common:5; Rare:66 | ||||
| chr6:80106383-80106715 | Common:2; Rare:113; Clinvar (pathogenic):1 | ||||
| chr6:80106858-80107262 | Common:3; Rare:168; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr6:81751755-81752221 | Common:4; Rare:291; Clinvar (pathogenic):1 | ||||
| chr6:81752668-81752864 | Rare:99 | ||||
| chr6:82247225-82247348 | Rare:19 | ||||
| chr6:82247701-82248041 | Common:1; Rare:103 | ||||
| chr6:82363514-82363888 | Common:3; Rare:118 | ||||
| chr6:82364138-82364321 | Common:2; Rare:46 | ||||
| chr6:83065341-83065750 | Common:1; Rare:176 | ||||
| chr6:83067567-83067756 | Common:1; Rare:57 | ||||
| chr6:83193199-83193440 | Common:3; Rare:79 |