Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:31958902-31959179 | Rare:86; Clinvar:8 | ||||
chr6:32178309-32178505 | Rare:36 | ||||
chr6:32843994-32844126 | Rare:30; Clinvar:1 | ||||
chr6:32844616-32844840 | Common:1; Rare:48 | ||||
chr6:32853680-32853799 | Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
chr6:32854024-32854227 | Common:2; Rare:53 | ||||
chr6:32968491-32968602 | Common:1; Rare:32 | ||||
chr6:33200656-33200920 | Common:2; Rare:81 | ||||
chr6:33271678-33272122 | Common:2; Rare:156 | ||||
chr6:33289186-33289397 | Common:2; Rare:50 | ||||
chr6:33298930-33299032 | Rare:26 | ||||
chr6:33454406-33454586 | Rare:50 | ||||
chr6:34696738-34696972 | Common:1; Rare:53 | ||||
chr6:36442910-36443077 | Common:2; Rare:66 | ||||
chr6:37257635-37257774 | Rare:37 |