Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:157044991-157045298 | Common:3; Rare:55 | ||||
chr1:157045610-157046300 | Common:2; Rare:684 | ||||
chr1:157138277-157138858 | Common:22; Rare:617 | ||||
chr1:157138797-157139248 | Common:4; Rare:235 | ||||
chr1:158685941-158686341 | Common:4; Rare:114 | ||||
chr1:158686510-158686930 | Common:22; Rare:160; Clinvar:3; Clinvar (benign):6 | ||||
chr1:159005833-159006233 | Common:5; Rare:96 | ||||
chr1:159009827-159010227 | Common:4; Rare:179 | ||||
chr1:159015312-159015865 | Common:5; Rare:287 | ||||
chr1:159076494-159077221 | Common:9; Rare:199 | ||||
chr1:159077153-159077600 | Common:8; Rare:213 | ||||
chr1:159203639-159204039 | Common:2; Rare:86 | ||||
chr1:159204080-159204738 | Common:13; Rare:232 | ||||
chr1:159204749-159205481 | Common:8; Rare:279; Clinvar (pathogenic):2 | ||||
chr1:159780635-159781035 | Common:17; Rare:254 |