Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23019336-23019517 | Rare:59 | ||||
chr1:23368333-23368502 | Common:1; Rare:38 | ||||
chr1:23424594-23424946 | Common:1; Rare:93 | ||||
chr1:23531211-23531442 | Common:2; Rare:28 | ||||
chr1:23559408-23559643 | Common:1; Rare:101 | ||||
chr1:23777953-23778106 | Rare:29 | ||||
chr1:23778281-23778440 | Common:6; Rare:81 | ||||
chr1:23800723-23800938 | Common:1; Rare:73 | ||||
chr1:23825385-23825543 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:23959641-23959873 | Common:2; Rare:66 | ||||
chr1:23980193-23980525 | Rare:89 | ||||
chr1:24556013-24556141 | Common:2; Rare:38 | ||||
chr1:24642882-24643350 | Common:2; Rare:153 | ||||
chr1:25232442-25232644 | Rare:83 | ||||
chr1:25247076-25247125 | Rare:11 |