Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32351350-32351639 | Common:1; Rare:79 | ||||
chr1:32394385-32394680 | Common:1; Rare:89 | ||||
chr1:32650513-32650651 | Common:1; Rare:66 | ||||
chr1:32650918-32651318 | Common:2; Rare:150 | ||||
chr1:32817240-32817686 | Rare:119; Clinvar:5; Clinvar (benign):1 | ||||
chr1:33080992-33081158 | Common:2; Rare:38 | ||||
chr1:34985292-34985379 | Common:1; Rare:32 | ||||
chr1:35190495-35190891 | Rare:111 | ||||
chr1:35192494-35192723 | Common:1; Rare:74 | ||||
chr1:35193092-35193420 | Common:2; Rare:111 | ||||
chr1:35557346-35557456 | Rare:31 | ||||
chr1:35557597-35557850 | Common:2; Rare:99 | ||||
chr1:35641386-35641629 | Rare:55 | ||||
chr1:35930803-35931274 | Common:2; Rare:166 | ||||
chr1:36149415-36149753 | Common:2; Rare:95 |