Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9244770-9245072 | Common:2; Rare:81; Clinvar (benign):1 | ||||
chr1:9687503-9687633 | Common:1; Rare:33 | ||||
chr1:12619107-12619160 | Rare:16 | ||||
chr1:13619981-13620117 | Common:5; Rare:21 | ||||
chr1:13620135-13620433 | Common:2; Rare:61 | ||||
chr1:13893007-13893239 | Common:1; Rare:67 | ||||
chr1:13949182-13949341 | Common:3; Rare:24 | ||||
chr1:15834859-15834957 | Common:1; Rare:43 | ||||
chr1:15835802-15836134 | Common:6; Rare:161 | ||||
chr1:15849405-15849647 | Common:1; Rare:58 | ||||
chr1:16155015-16155223 | Rare:44 | ||||
chr1:16217419-16217647 | Rare:36 | ||||
chr1:16644644-16644745 | Common:1; Rare:2 | ||||
chr1:16895690-16895986 | Common:4; Rare:57 | ||||
chr1:16904815-16904950 | Common:2; Rare:17 |