Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40040457-40040799 | Common:3; Rare:103 | ||||
chr1:40097234-40097316 | Rare:33; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40161265-40161395 | Rare:35 | ||||
chr1:40257895-40258272 | Common:4; Rare:104; Clinvar:8 | ||||
chr1:40374576-40374667 | Common:12; Rare:23 | ||||
chr1:40449932-40450159 | Common:4; Rare:93 | ||||
chr1:40508681-40508787 | Common:3; Rare:28 | ||||
chr1:40531514-40531668 | Rare:35 | ||||
chr1:40691495-40691822 | Common:3; Rare:157 | ||||
chr1:40692045-40692176 | Rare:47 | ||||
chr1:40709191-40709377 | Rare:47 | ||||
chr1:42335149-42335304 | Common:1; Rare:75 | ||||
chr1:42456036-42456380 | Common:1; Rare:85 | ||||
chr1:42456473-42456568 | Rare:45 | ||||
chr1:42456843-42456963 | Common:1; Rare:47; Clinvar (pathogenic):1 |