Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:74733379-74733488 | Rare:43 | ||||
chr1:74733393-74734229 | Common:6; Rare:200 | ||||
chr1:75724160-75725886 | Common:65; Rare:1515; Clinvar:40; Clinvar (benign):31; Clinvar (pathogenic):2 | ||||
chr1:75732301-75732992 | Common:8; Rare:248; Clinvar:12; Clinvar (benign):6; Clinvar (pathogenic):14 | ||||
chr1:75785374-75786494 | Common:26; Rare:1118 | ||||
chr1:75786694-75786809 | Common:2; Rare:50 | ||||
chr1:75796374-75796921 | Common:2; Rare:251 | ||||
chr1:76074460-76074860 | Common:10; Rare:411 | ||||
chr1:77218773-77219061 | Common:3; Rare:47 | ||||
chr1:77219210-77219670 | Common:4; Rare:622 | ||||
chr1:77682096-77682937 | Common:5; Rare:375 | ||||
chr1:77682875-77683161 | Common:3; Rare:109 | ||||
chr1:77683280-77683840 | Common:6; Rare:566 | ||||
chr1:77758943-77759343 | Rare:127 | ||||
chr1:77759272-77760098 | Common:23; Rare:656 |