Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23980189-23980537 | Common:1; Rare:94 | ||||
chr1:24413714-24413849 | Common:1; Rare:26 | ||||
chr1:24415529-24415829 | Common:3; Rare:77 | ||||
chr1:24642875-24643316 | Common:1; Rare:147 | ||||
chr1:25232428-25232662 | Rare:94 | ||||
chr1:25247445-25247638 | Common:2; Rare:69 | ||||
chr1:25338232-25338459 | Common:2; Rare:78 | ||||
chr1:25819858-25820237 | Common:5; Rare:113 | ||||
chr1:25859368-25859580 | Common:2; Rare:85 | ||||
chr1:25905055-25905229 | Rare:26 | ||||
chr1:25906392-25906611 | Rare:83 | ||||
chr1:26111069-26111226 | Rare:49 | ||||
chr1:26279953-26280158 | Rare:120 | ||||
chr1:26306626-26306837 | Common:10; Rare:55 | ||||
chr1:26432112-26432412 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):1 |