Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:198935137-198935475 | Common:1; Rare:65 | ||||
chr1:198937374-198937495 | Common:2; Rare:26 | ||||
chr1:200738764-200738993 | Common:6; Rare:80 | ||||
chr1:201000464-201000781 | Common:2; Rare:107 | ||||
chr1:202810753-202810961 | Common:1; Rare:67 | ||||
chr1:202861524-202861755 | Common:1; Rare:64 | ||||
chr1:204288359-204288588 | Common:1; Rare:43 | ||||
chr1:204350913-204351083 | Rare:34 | ||||
chr1:209623162-209623383 | Common:1; Rare:46; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:210233784-210234051 | Common:8; Rare:88 | ||||
chr1:210234141-210234303 | Common:3; Rare:39 | ||||
chr1:211382609-211382861 | Common:2; Rare:96 | ||||
chr1:213986123-213986409 | Common:1; Rare:71 | ||||
chr1:218345202-218345405 | Common:1; Rare:36; Clinvar (benign):1 | ||||
chr1:222711464-222711629 | Rare:33 |