Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23778269-23778575 | Common:10; Rare:133 | ||||
chr1:23791066-23791231 | Rare:51 | ||||
chr1:23825411-23825537 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959641-23959868 | Common:2; Rare:63 | ||||
chr1:23979931-23980019 | Rare:32 | ||||
chr1:24413697-24413875 | Common:1; Rare:43 | ||||
chr1:24642890-24643329 | Common:2; Rare:146 | ||||
chr1:25232442-25232663 | Rare:90 | ||||
chr1:25247441-25247707 | Common:4; Rare:94 | ||||
chr1:25338190-25338447 | Common:1; Rare:91 | ||||
chr1:25819844-25820237 | Common:7; Rare:118 | ||||
chr1:25859387-25859630 | Common:1; Rare:91 | ||||
chr1:26279933-26280192 | Rare:141 | ||||
chr1:26432085-26432415 | Common:5; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26787877-26788195 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2 |