Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119768866-119769016 | Rare:28; Clinvar:1 | ||||
chr1:119896465-119896573 | Common:1; Rare:34 | ||||
chr1:120069513-120069828 | Common:5; Rare:83 | ||||
chr1:120176310-120176585 | Rare:58 | ||||
chr1:121184790-121185067 | Common:1; Rare:97 | ||||
chr1:145405496-145405647 | Common:1; Rare:17 | ||||
chr1:145607840-145608069 | Common:2; Rare:71 | ||||
chr1:145823870-145824327 | Rare:151 | ||||
chr1:145839382-145839510 | Rare:24 | ||||
chr1:145845331-145845642 | Common:4; Rare:77 | ||||
chr1:145858992-145859068 | Rare:26 | ||||
chr1:145859070-145859169 | Rare:23 | ||||
chr1:145859741-145860123 | Common:4; Rare:101 | ||||
chr1:145918463-145919043 | Common:3; Rare:137; Clinvar:2; Clinvar (benign):1 | ||||
chr1:145927028-145927180 | Rare:40 |