Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:46860910-46861111 | Common:1; Rare:69 | ||||
chr19:48966277-48966643 | Rare:115; Clinvar (pathogenic):2 | ||||
chr19:52942556-52942782 | Common:7; Rare:82 | ||||
chr19:52993524-52993783 | Common:3; Rare:54 | ||||
chr19:58575332-58575472 | Rare:42 | ||||
chr2:19348021-19348114 | Common:1; Rare:30 | ||||
chr2:21029769-21029987 | Rare:59; Clinvar:1; Clinvar (benign):7 | ||||
chr2:27752758-27752917 | Rare:24 | ||||
chr2:88016539-88016802 | Common:9; Rare:112 | ||||
chr2:170770766-170771101 | Common:2; Rare:58 | ||||
chr2:185424894-185425112 | Common:6; Rare:71 | ||||
chr2:193502495-193502843 | Common:9; Rare:118 | ||||
chr2:202376105-202376151 | Rare:20 | ||||
chr2:240456692-240456722 | Rare:9 | ||||
chr20:6704264-6704485 | Rare:29 |