Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:22451742-22451868 | Common:1; Rare:51 | ||||
chr1:23344233-23344532 | Common:2; Rare:96 | ||||
chr1:23368281-23368508 | Common:1; Rare:62 | ||||
chr1:23368854-23369002 | Common:1; Rare:50 | ||||
chr1:23369191-23369254 | Rare:16 | ||||
chr1:23369815-23369938 | Rare:22 | ||||
chr1:23559479-23559648 | Common:1; Rare:69 | ||||
chr1:23691749-23691826 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23778275-23778659 | Common:10; Rare:144 | ||||
chr1:23800745-23800948 | Common:1; Rare:67 | ||||
chr1:23825411-23825534 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959641-23959854 | Common:2; Rare:57 | ||||
chr1:23980191-23980501 | Rare:81 | ||||
chr1:24413714-24413868 | Common:1; Rare:35 | ||||
chr1:24415633-24415812 | Common:1; Rare:53 |