Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10033415-10033513 | Rare:14 | ||||
chr1:10210246-10210661 | Common:7; Rare:120 | ||||
chr1:10210854-10211076 | Common:1; Rare:65; Clinvar (benign):1 | ||||
chr1:10211521-10211583 | Common:1; Rare:10 | ||||
chr1:10211860-10212086 | Common:1; Rare:42 | ||||
chr1:10398585-10398604 | Rare:2 | ||||
chr1:10398767-10399133 | Common:2; Rare:137 | ||||
chr1:10399253-10399441 | Common:2; Rare:42 | ||||
chr1:10430306-10430515 | Common:6; Rare:60 | ||||
chr1:10430606-10430826 | Common:6; Rare:76 | ||||
chr1:10430968-10431009 | Rare:11 | ||||
chr1:10471855-10471956 | Rare:19 | ||||
chr1:10472368-10472773 | Rare:106 | ||||
chr1:10474784-10475235 | Common:1; Rare:142; Clinvar:4; Clinvar (benign):1 | ||||
chr1:10475341-10475427 | Common:1; Rare:22 |