Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:75243738-75243966 | Common:1; Rare:103 | ||||
chr6:75284634-75285020 | Common:1; Rare:120 | ||||
chr6:75601808-75601902 | Rare:39 | ||||
chr6:79078138-79078523 | Common:1; Rare:168 | ||||
chr6:79537386-79537540 | Common:1; Rare:38; Clinvar:2 | ||||
chr6:79631175-79631330 | Common:2; Rare:38 | ||||
chr6:81752660-81752830 | Rare:88 | ||||
chr6:83193222-83193383 | Common:3; Rare:57 | ||||
chr6:85593819-85593987 | Rare:57 | ||||
chr6:85643823-85643931 | Common:2; Rare:34 | ||||
chr6:87155268-87155620 | Rare:100 | ||||
chr6:87589953-87590160 | Common:2; Rare:91; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr6:88963585-88963830 | Common:2; Rare:83 | ||||
chr6:89080882-89081021 | Common:1; Rare:53 | ||||
chr6:89081048-89081387 | Common:2; Rare:130 |