Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:224434792-224434966 | Rare:46 | ||||
chr1:225427958-225428280 | Common:3; Rare:110; Clinvar:5; Clinvar (benign):3 | ||||
chr1:225652484-225653057 | Common:3; Rare:150 | ||||
chr1:225777716-225778011 | Common:3; Rare:100 | ||||
chr1:225865788-225865985 | Common:1; Rare:62 | ||||
chr1:225866169-225866365 | Rare:32 | ||||
chr1:225866758-225866921 | Rare:27 | ||||
chr1:225882296-225882464 | Rare:49 | ||||
chr1:225999192-225999618 | Common:2; Rare:154 | ||||
chr1:226062024-226062094 | Common:1; Rare:22 | ||||
chr1:226062481-226062828 | Rare:119 | ||||
chr1:226186449-226186786 | Common:1; Rare:97 | ||||
chr1:226309111-226309369 | Common:1; Rare:118 | ||||
chr1:226407808-226407830 | Rare:6 | ||||
chr1:226407917-226408233 | Common:2; Rare:102 |