Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:40605516-40605916 | Common:2; Rare:221; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr19:40607710-40608170 | Common:3; Rare:128 | ||||
chr19:40736121-40736421 | Common:6; Rare:87 | ||||
chr19:41327380-41327730 | Common:4; Rare:112 | ||||
chr19:41327750-41328070 | Common:4; Rare:139 | ||||
chr19:41352490-41352738 | Common:3; Rare:116 | ||||
chr19:41352937-41353127 | Common:4; Rare:65; Clinvar (benign):2 | ||||
chr19:42396907-42397204 | Common:2; Rare:138 | ||||
chr19:43324175-43324434 | Common:1; Rare:28 | ||||
chr19:43325519-43325755 | Common:3; Rare:33 | ||||
chr19:43325660-43326200 | Common:5; Rare:99 | ||||
chr19:43326460-43326816 | Common:4; Rare:59 | ||||
chr19:43327886-43328391 | Common:6; Rare:145 | ||||
chr19:43328385-43328493 | Rare:5 | ||||
chr19:43331486-43331664 | Common:1; Rare:36 |