Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:165698444-165698747 | Common:5; Rare:123 | ||||
chr1:165768732-165769030 | Common:2; Rare:114 | ||||
chr1:166975347-166975612 | Common:2; Rare:79 | ||||
chr1:167721808-167722207 | Common:3; Rare:94 | ||||
chr1:167935898-167936327 | Common:2; Rare:120 | ||||
chr1:167936556-167936974 | Common:1; Rare:147 | ||||
chr1:168178724-168179110 | Common:4; Rare:119 | ||||
chr1:168225913-168226086 | Common:2; Rare:62 | ||||
chr1:169367773-169368256 | Common:3; Rare:91 | ||||
chr1:169485694-169485860 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):4 | ||||
chr1:169485919-169486219 | Common:1; Rare:77; Clinvar:2 | ||||
chr1:169794872-169795045 | Common:3; Rare:35 | ||||
chr1:169893655-169893717 | Rare:17 | ||||
chr1:170074474-170074752 | Common:1; Rare:80 | ||||
chr1:170532068-170532201 | Rare:71; Clinvar:1 |