Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244652961-244653227 | Common:2; Rare:105 | ||||
chr1:244834958-244835368 | Rare:136 | ||||
chr1:244835554-244835750 | Common:2; Rare:86; Clinvar (benign):5 | ||||
chr1:244856455-244856857 | Common:1; Rare:80; Clinvar (benign):2 | ||||
chr1:244862938-244863273 | Common:4; Rare:131 | ||||
chr1:244863927-244864728 | Common:2; Rare:282; Clinvar:4; Clinvar (benign):6 | ||||
chr1:244970051-244970204 | Common:1; Rare:55 | ||||
chr1:244970251-244970438 | Common:3; Rare:88 | ||||
chr1:244970916-244971117 | Common:1; Rare:60 | ||||
chr1:246305926-246306313 | Common:2; Rare:65 | ||||
chr1:246507221-246507380 | Common:1; Rare:63 | ||||
chr1:246566140-246566630 | Common:3; Rare:159 | ||||
chr1:246723884-246724064 | Common:1; Rare:35 | ||||
chr1:246724242-246724611 | Common:2; Rare:127 | ||||
chr1:246931678-246931802 | Common:1; Rare:32 |