Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593631-63593909 | Common:2; Rare:125; Clinvar (pathogenic):1 | ||||
chr1:63594187-63594378 | Common:3; Rare:44 | ||||
chr1:64864129-64864379 | Rare:42 | ||||
chr1:64966002-64966180 | Rare:51 | ||||
chr1:64966446-64966771 | Common:3; Rare:121 | ||||
chr1:65147945-65148214 | Common:4; Rare:63 | ||||
chr1:65148879-65149008 | Common:1; Rare:37 | ||||
chr1:65149083-65149112 | Rare:4 | ||||
chr1:65254319-65254462 | Common:2; Rare:56 | ||||
chr1:65420419-65420820 | Common:7; Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
chr1:65420905-65420979 | Rare:16 | ||||
chr1:66332127-66332307 | Rare:34 | ||||
chr1:66332401-66332472 | Rare:29 | ||||
chr1:66924817-66925079 | Rare:106 | ||||
chr1:66925155-66925521 | Common:2; Rare:116 |