Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173836805-173837042 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr1:173863924-173863992 | Rare:17 | ||||
chr1:173864056-173864111 | Rare:19 | ||||
chr1:173864322-173864500 | Rare:70 | ||||
chr1:173864530-173864692 | Rare:30 | ||||
chr1:173864696-173864757 | Rare:18 | ||||
chr1:173864866-173865025 | Common:2; Rare:57 | ||||
chr1:173865189-173865315 | Common:2; Rare:32 | ||||
chr1:173865509-173865588 | Common:1; Rare:15 | ||||
chr1:173865845-173865960 | Rare:37 | ||||
chr1:173866063-173866415 | Common:3; Rare:126 | ||||
chr1:173866698-173866873 | Common:1; Rare:68 | ||||
chr1:173866964-173867062 | Common:1; Rare:27 | ||||
chr1:174514268-174514279 | Rare:1 | ||||
chr1:174539440-174539540 | Common:1; Rare:21 |