Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62784032-62784228 | Rare:182 | ||||
chr1:63322389-63322605 | Rare:176 | ||||
chr1:63367437-63367806 | Common:2; Rare:251; Clinvar (benign):3 | ||||
chr1:63523126-63523621 | Common:9; Rare:386 | ||||
chr1:63592900-63593470 | Rare:221; Clinvar (benign):2 | ||||
chr1:63593510-63593901 | Common:4; Rare:330; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr1:63594399-63594513 | Common:1; Rare:23 | ||||
chr1:63773750-63774140 | Rare:76 | ||||
chr1:64470013-64470305 | Common:3; Rare:72 | ||||
chr1:64505477-64505806 | Common:2; Rare:43 | ||||
chr1:64744200-64744660 | Common:2; Rare:130 | ||||
chr1:64744788-64745213 | Common:4; Rare:304 | ||||
chr1:64965796-64966202 | Common:2; Rare:154 | ||||
chr1:64966278-64966790 | Common:8; Rare:387 | ||||
chr1:65147439-65147710 | Common:2; Rare:124 |