Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54887168-54887418 | Common:3; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
chr1:58783973-58784153 | Rare:44 | ||||
chr1:59296520-59296834 | Common:12; Rare:82 | ||||
chr1:61076986-61077230 | Common:3; Rare:64 | ||||
chr1:62436262-62436385 | Common:2; Rare:38 | ||||
chr1:62688277-62688504 | Common:1; Rare:93 | ||||
chr1:63367521-63367668 | Rare:43 | ||||
chr1:63523179-63523592 | Common:3; Rare:105 | ||||
chr1:63593337-63593472 | Rare:55; Clinvar (benign):1 | ||||
chr1:66924800-66925023 | Rare:96 | ||||
chr1:66925182-66925503 | Common:2; Rare:103 | ||||
chr1:66930054-66930391 | Rare:113 | ||||
chr1:67429989-67430241 | Rare:90 | ||||
chr1:70205549-70205769 | Rare:69 | ||||
chr1:70354671-70354842 | Rare:61 |