Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:204114365-204114598 | Rare:60 | ||||
chr1:204410084-204410369 | Common:1; Rare:77 | ||||
chr1:204410416-204410715 | Common:1; Rare:100 | ||||
chr1:207752702-207752743 | Rare:8 | ||||
chr1:209673243-209673554 | Rare:56 | ||||
chr1:209706745-209707133 | Common:2; Rare:107; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr1:209724383-209724609 | Common:1; Rare:37 | ||||
chr1:211382666-211382886 | Common:1; Rare:88 | ||||
chr1:211829205-211829586 | Common:1; Rare:78 | ||||
chr1:211890166-211890304 | Common:1; Rare:39 | ||||
chr1:213986104-213986183 | Rare:23 | ||||
chr1:213986184-213986393 | Common:1; Rare:49 | ||||
chr1:221549080-221549432 | Common:8; Rare:68 | ||||
chr1:221563477-221563796 | Common:3; Rare:66 | ||||
chr1:223750803-223750974 | Common:1; Rare:46 |