Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62436800-62437102 | Common:1; Rare:77 | ||||
chr1:62688266-62688543 | Common:1; Rare:106 | ||||
chr1:62784050-62784200 | Rare:58 | ||||
chr1:63367482-63367675 | Rare:59; Clinvar (benign):1 | ||||
chr1:63523160-63523592 | Common:3; Rare:119 | ||||
chr1:63593060-63593460 | Rare:115; Clinvar (benign):1 | ||||
chr1:63594441-63594648 | Common:4; Rare:44 | ||||
chr1:64841243-64841569 | Rare:77; Clinvar:2 | ||||
chr1:64846638-64846809 | Common:1; Rare:50; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:66332139-66332368 | Rare:46 | ||||
chr1:66332370-66332618 | Rare:67 | ||||
chr1:66924820-66925042 | Rare:93 | ||||
chr1:66925188-66925525 | Common:2; Rare:104 | ||||
chr1:67053925-67054169 | Common:1; Rare:92 | ||||
chr1:67429993-67430311 | Rare:106 |