Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236065037-236065360 | Common:3; Rare:122; Clinvar (pathogenic):1 | ||||
chr1:236281936-236282112 | Common:3; Rare:50 | ||||
chr1:241848121-241848255 | Common:1; Rare:24 | ||||
chr1:243255046-243255422 | Common:1; Rare:86 | ||||
chr1:243255783-243256107 | Rare:86; Clinvar:4 | ||||
chr1:244451807-244452174 | Common:1; Rare:128 | ||||
chr1:244835197-244835327 | Rare:58 | ||||
chr1:244864386-244864686 | Rare:115 | ||||
chr1:246566209-246566587 | Common:1; Rare:123 | ||||
chr1:247171998-247172048 | Common:1; Rare:7 | ||||
chr1:248858940-248859146 | Rare:80 | ||||
chr10:650002-650060 | Rare:10 | ||||
chr10:988363-988492 | Common:1; Rare:54 | ||||
chr10:1048880-1049086 | Common:2; Rare:108 | ||||
chr10:1056702-1056878 | Common:3; Rare:63 |