Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62436766-62437110 | Common:1; Rare:95 | ||||
chr1:62688260-62688545 | Common:1; Rare:108; Clinvar:1 | ||||
chr1:62784070-62784193 | Rare:51 | ||||
chr1:63367517-63367692 | Rare:53; Clinvar (benign):1 | ||||
chr1:63523161-63523602 | Common:3; Rare:119 | ||||
chr1:65147535-65147653 | Rare:34 | ||||
chr1:66332152-66332441 | Rare:63 | ||||
chr1:66924845-66925035 | Rare:80 | ||||
chr1:66925199-66925525 | Common:2; Rare:100 | ||||
chr1:66930082-66930394 | Rare:100 | ||||
chr1:67429989-67430127 | Rare:49 | ||||
chr1:67430131-67430600 | Rare:173 | ||||
chr1:67833335-67833504 | Common:2; Rare:68 | ||||
chr1:68232476-68232633 | Rare:37 | ||||
chr1:68497023-68497297 | Common:3; Rare:91 |