Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:159726948-159727203 | Rare:92 | ||||
chr6:159727333-159727694 | Common:5; Rare:146 | ||||
chr6:159789514-159789966 | Common:4; Rare:152 | ||||
chr6:159790272-159790516 | Common:7; Rare:81 | ||||
chr6:160991643-160991785 | Common:1; Rare:47 | ||||
chr6:163415109-163415331 | Common:6; Rare:83 | ||||
chr6:166342519-166342665 | Common:3; Rare:55 | ||||
chr6:166382819-166383097 | Common:2; Rare:96; Clinvar (benign):1 | ||||
chr6:166627970-166628253 | Common:1; Rare:60 | ||||
chr6:166999081-166999406 | Common:1; Rare:111 | ||||
chr6:167966586-167966860 | Common:3; Rare:60 | ||||
chr6:169702004-169702196 | Common:3; Rare:99 | ||||
chr6:169751497-169751645 | Rare:58; Clinvar (benign):1 | ||||
chr6:170553129-170553353 | Common:2; Rare:95 | ||||
chr6:170554186-170554461 | Common:2; Rare:82 |