Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:3977208-3977612 | Common:4; Rare:131; Clinvar (benign):8 | ||||
chr19:4058375-4058583 | Common:2; Rare:61 | ||||
chr19:4061308-4061460 | Common:4; Rare:38 | ||||
chr19:4793307-4793346 | Rare:11 | ||||
chr19:5844791-5845259 | Common:2; Rare:99 | ||||
chr19:6742953-6743539 | Common:3; Rare:170 | ||||
chr19:7611532-7611727 | Rare:68 | ||||
chr19:9674288-9674326 | Rare:10 | ||||
chr19:10555163-10555212 | Rare:15 | ||||
chr19:12793558-12793737 | Common:3; Rare:44 | ||||
chr19:13840699-13840896 | Common:1; Rare:40 | ||||
chr19:13887214-13887389 | Common:5; Rare:38 | ||||
chr19:14554562-14554753 | Common:3; Rare:29 | ||||
chr19:14565950-14566082 | Common:1; Rare:53 | ||||
chr19:15227551-15227856 | Rare:110 |