Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62784047-62784180 | Rare:50 | ||||
chr1:63523152-63523592 | Common:3; Rare:121 | ||||
chr1:63593219-63593469 | Rare:92; Clinvar (benign):1 | ||||
chr1:64966409-64966658 | Common:1; Rare:90 | ||||
chr1:66924800-66925023 | Rare:96 | ||||
chr1:66925194-66925514 | Common:2; Rare:100 | ||||
chr1:67429993-67430467 | Rare:180 | ||||
chr1:68232510-68232627 | Rare:27 | ||||
chr1:70205542-70205770 | Rare:72 | ||||
chr1:70221276-70221518 | Rare:103 | ||||
chr1:70354680-70354838 | Rare:56 | ||||
chr1:70411023-70411279 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080982-71081367 | Rare:103 | ||||
chr1:74198125-74198324 | Common:2; Rare:110 | ||||
chr1:74733001-74733266 | Common:5; Rare:85 |