Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
chr18:49813891-49814206 | Common:1; Rare:139 | ||||
chr18:56651132-56651402 | Common:4; Rare:70 | ||||
chr18:58864745-58864885 | Rare:30 | ||||
chr18:59273359-59273514 | Rare:42 | ||||
chr18:62186974-62187320 | Common:5; Rare:97 | ||||
chr18:63422396-63422686 | Common:2; Rare:81 | ||||
chr18:68715030-68715250 | Common:4; Rare:101 | ||||
chr18:70205659-70205936 | Common:4; Rare:103; Clinvar (benign):2 | ||||
chr18:74148358-74148543 | Common:1; Rare:57 | ||||
chr18:74496021-74496402 | Common:4; Rare:122 | ||||
chr18:74597579-74597931 | Common:2; Rare:98 | ||||
chr19:572342-572644 | Rare:168 | ||||
chr19:633508-633727 | Common:8; Rare:108 | ||||
chr19:893173-893484 | Common:3; Rare:132 |