Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:220879687-220879734 | Rare:13 | ||||
chr1:221742065-221742325 | Common:1; Rare:75 | ||||
chr1:222589871-222590037 | Common:2; Rare:44 | ||||
chr1:222644159-222644392 | Common:1; Rare:68 | ||||
chr1:222712437-222712850 | Common:3; Rare:142 | ||||
chr1:223143219-223143336 | Common:2; Rare:31 | ||||
chr1:224182908-224183324 | Common:3; Rare:149 | ||||
chr1:224330121-224330439 | Common:6; Rare:97 | ||||
chr1:224433689-224433784 | Rare:19 | ||||
chr1:224434792-224434966 | Rare:46 | ||||
chr1:225427968-225428329 | Common:3; Rare:128; Clinvar:5; Clinvar (benign):3 | ||||
chr1:225777696-225777895 | Common:3; Rare:58 | ||||
chr1:225882320-225882483 | Rare:49 | ||||
chr1:225999309-225999629 | Common:2; Rare:110 | ||||
chr1:226062028-226062094 | Common:1; Rare:22 |