Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:2087634-2087776 | Rare:16 | ||||
chr19:2168317-2168587 | Common:3; Rare:66 | ||||
chr19:2246724-2246767 | Rare:14 | ||||
chr19:2289981-2290001 | Common:1; Rare:7 | ||||
chr19:2326172-2326294 | Common:2; Rare:21 | ||||
chr19:2332369-2332661 | Common:1; Rare:59 | ||||
chr19:2680939-2681102 | Common:1; Rare:42 | ||||
chr19:3179949-3180313 | Common:1; Rare:89 | ||||
chr19:3181589-3181884 | Common:3; Rare:63 | ||||
chr19:3552937-3553087 | Rare:22 | ||||
chr19:3977214-3977607 | Common:4; Rare:128; Clinvar (benign):8 | ||||
chr19:4035827-4036037 | Common:17; Rare:29 | ||||
chr19:4115065-4115192 | Rare:32 | ||||
chr19:4915354-4915389 | Rare:9 | ||||
chr19:4977368-4977638 | Common:1; Rare:70 |