Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23559434-23559643 | Common:1; Rare:92 | ||||
chr1:23691726-23691829 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
chr1:23791066-23791247 | Rare:55 | ||||
chr1:23791832-23791991 | Rare:32 | ||||
chr1:23825403-23825543 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959670-23959908 | Common:2; Rare:58 | ||||
chr1:23980190-23980604 | Common:1; Rare:114 | ||||
chr1:24187254-24187436 | Common:2; Rare:43 | ||||
chr1:24413690-24413897 | Common:1; Rare:47 | ||||
chr1:24415501-24415827 | Common:3; Rare:80 | ||||
chr1:24642911-24643329 | Common:2; Rare:139 | ||||
chr1:25232444-25232668 | Rare:92 | ||||
chr1:25247445-25247638 | Common:2; Rare:69 | ||||
chr1:25338180-25338431 | Common:1; Rare:92 | ||||
chr1:25819866-25820023 | Common:2; Rare:50 |