Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25247413-25247638 | Common:2; Rare:86 | ||||
chr1:25337805-25337951 | Rare:20 | ||||
chr1:25338214-25338479 | Common:2; Rare:87 | ||||
chr1:25819892-25820021 | Common:2; Rare:40 | ||||
chr1:25859370-25859542 | Common:2; Rare:70 | ||||
chr1:25906397-25906573 | Rare:71 | ||||
chr1:26279859-26280191 | Rare:180 | ||||
chr1:26432253-26432390 | Common:3; Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472204-26472532 | Common:4; Rare:103 | ||||
chr1:26472585-26472627 | Rare:13 | ||||
chr1:26787874-26788214 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890258-26890359 | Common:1; Rare:35 | ||||
chr1:26900432-26900524 | Rare:35 | ||||
chr1:26960377-26960458 | Common:1; Rare:16 | ||||
chr1:27725758-27726008 | Common:2; Rare:68 |