Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23791066-23791247 | Rare:55 | ||||
chr1:23800723-23800959 | Common:1; Rare:84 | ||||
chr1:23825405-23825534 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959585-23959881 | Common:3; Rare:80 | ||||
chr1:23979933-23980058 | Common:2; Rare:36 | ||||
chr1:23980189-23980525 | Rare:89 | ||||
chr1:24187254-24187428 | Common:2; Rare:40 | ||||
chr1:24413691-24413855 | Common:1; Rare:36 | ||||
chr1:24415530-24415812 | Common:3; Rare:75 | ||||
chr1:24642890-24643326 | Common:2; Rare:146 | ||||
chr1:24745548-24745622 | Rare:22 | ||||
chr1:25232442-25232662 | Rare:89 | ||||
chr1:25247412-25247640 | Common:2; Rare:88 | ||||
chr1:25337838-25337948 | Rare:12 | ||||
chr1:25338156-25338487 | Common:2; Rare:109 |