Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38873296-38873563 | Common:3; Rare:93 | ||||
chr1:39026246-39026398 | Common:1; Rare:41 | ||||
chr1:39883467-39883575 | Rare:42; Clinvar (pathogenic):1 | ||||
chr1:40040444-40040819 | Common:3; Rare:116 | ||||
chr1:40161276-40161402 | Rare:32 | ||||
chr1:40257889-40258282 | Common:4; Rare:108; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40508626-40508813 | Common:6; Rare:57 | ||||
chr1:40531514-40531876 | Common:2; Rare:72 | ||||
chr1:40531972-40532085 | Rare:19 | ||||
chr1:40691452-40691862 | Common:3; Rare:177 | ||||
chr1:40692036-40692197 | Common:1; Rare:55 | ||||
chr1:40709166-40709369 | Rare:49 | ||||
chr1:42335157-42335386 | Common:5; Rare:111 | ||||
chr1:42455993-42456124 | Rare:45 | ||||
chr1:42456258-42456594 | Common:1; Rare:109 |