Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:54102678-54102887 | Common:3; Rare:56 | ||||
chr19:54115280-54115402 | Common:1; Rare:27; Clinvar (benign):1 | ||||
chr19:54115613-54115812 | Common:3; Rare:50; Clinvar:5; Clinvar (benign):1 | ||||
chr19:54200718-54200891 | Common:2; Rare:67 | ||||
chr19:54449039-54449247 | Common:2; Rare:60 | ||||
chr19:55370439-55370745 | Common:3; Rare:67 | ||||
chr19:55385851-55385965 | Common:3; Rare:55 | ||||
chr19:55654848-55655079 | Rare:83 | ||||
chr19:56368276-56368336 | Rare:17 | ||||
chr19:57279842-57279995 | Rare:42 | ||||
chr19:57320387-57320509 | Common:2; Rare:39 | ||||
chr19:57435136-57435343 | Common:6; Rare:41 | ||||
chr19:57584007-57584120 | Common:1; Rare:21 | ||||
chr19:57814885-57815206 | Rare:77 | ||||
chr19:58278721-58278987 | Common:3; Rare:84 |