Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:76491492-76491654 | Common:3; Rare:67 | ||||
chr19:1876155-1876283 | Common:1; Rare:50 | ||||
chr19:2046233-2046438 | Common:3; Rare:86 | ||||
chr19:4705933-4706171 | Common:1; Rare:62 | ||||
chr19:4793996-4794038 | Rare:8 | ||||
chr19:6312157-6312444 | Common:2; Rare:102 | ||||
chr19:7608025-7608140 | Rare:25 | ||||
chr19:7611532-7611739 | Rare:69 | ||||
chr19:13023427-13023489 | Rare:14 | ||||
chr19:14070403-14070560 | Rare:37 | ||||
chr19:15185256-15185549 | Rare:85; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:15191802-15192049 | Common:1; Rare:84; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:15238912-15239196 | Common:2; Rare:97 | ||||
chr19:15828823-15829096 | Common:3; Rare:44 | ||||
chr19:19776378-19776596 | Common:2; Rare:60 |