Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23368177-23368502 | Common:1; Rare:97 | ||||
chr1:23368843-23368974 | Common:1; Rare:46 | ||||
chr1:23530824-23530994 | Common:1; Rare:37 | ||||
chr1:23531211-23531442 | Common:2; Rare:28 | ||||
chr1:23559419-23559651 | Common:1; Rare:97 | ||||
chr1:23778257-23778501 | Common:9; Rare:126 | ||||
chr1:23796766-23796804 | Rare:9; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:23799516-23799670 | Rare:26 | ||||
chr1:23800723-23800929 | Common:1; Rare:69 | ||||
chr1:23825400-23825535 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959607-23959916 | Common:2; Rare:82 | ||||
chr1:23980189-23980497 | Rare:79 | ||||
chr1:24319271-24319827 | Common:2; Rare:126 | ||||
chr1:24380024-24380111 | Rare:10 | ||||
chr1:24413461-24413548 | Common:1; Rare:15 |