Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63523192-63523584 | Common:3; Rare:100 | ||||
chr1:63593214-63593761 | Rare:232; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr1:64841243-64841529 | Rare:64; Clinvar:1 | ||||
chr1:66533391-66533609 | Common:2; Rare:28 | ||||
chr1:66533884-66534169 | Common:1; Rare:69 | ||||
chr1:66924838-66925023 | Rare:79 | ||||
chr1:66925207-66925514 | Common:2; Rare:97 | ||||
chr1:67429989-67430472 | Rare:184 | ||||
chr1:70205542-70205775 | Rare:73 | ||||
chr1:70354659-70354820 | Rare:52 | ||||
chr1:71080943-71081367 | Rare:112 | ||||
chr1:74198148-74198292 | Common:1; Rare:79 | ||||
chr1:74733030-74733334 | Common:6; Rare:111 | ||||
chr1:75732708-75732920 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
chr1:77219398-77219496 | Rare:44 |