Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:224330079-224330442 | Common:7; Rare:125 | ||||
chr1:225427974-225428316 | Common:3; Rare:123; Clinvar:4; Clinvar (benign):3 | ||||
chr1:225882318-225882460 | Rare:43 | ||||
chr1:225999296-225999618 | Common:2; Rare:112 | ||||
chr1:226062462-226062725 | Rare:81 | ||||
chr1:226186491-226186844 | Common:1; Rare:105 | ||||
chr1:226309132-226309369 | Common:1; Rare:108 | ||||
chr1:226407864-226408376 | Common:5; Rare:158 | ||||
chr1:226939984-226940323 | Rare:110; Clinvar:2 | ||||
chr1:227735191-227735498 | Common:5; Rare:178 | ||||
chr1:228082498-228082759 | Common:3; Rare:106 | ||||
chr1:228103317-228103502 | Common:1; Rare:59 | ||||
chr1:228109217-228109509 | Rare:93 | ||||
chr1:228139953-228140381 | Common:3; Rare:135 | ||||
chr1:228165559-228165804 | Rare:63; Clinvar (benign):1 |