Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46915722-46916135 | Common:4; Rare:133; Clinvar:2; Clinvar (benign):1 | ||||
chr2:47402962-47403180 | Common:1; Rare:97; Clinvar:29; Clinvar (benign):23 | ||||
chr2:48440616-48440787 | Common:5; Rare:70 | ||||
chr2:53767748-53767873 | Common:2; Rare:48 | ||||
chr2:53786842-53787175 | Common:1; Rare:125 | ||||
chr2:53970788-53971152 | Common:11; Rare:131 | ||||
chr2:55050298-55050398 | Rare:43 | ||||
chr2:55050441-55050784 | Common:4; Rare:103 | ||||
chr2:55232335-55232726 | Common:2; Rare:113 | ||||
chr2:55923711-55923835 | Common:3; Rare:43; Clinvar (benign):7 | ||||
chr2:58241316-58241396 | Rare:50; Clinvar:3; Clinvar (benign):1 | ||||
chr2:61017440-61017750 | Common:1; Rare:93; Clinvar:2 | ||||
chr2:61144921-61145164 | Common:3; Rare:82 | ||||
chr2:61470743-61470983 | Rare:66 | ||||
chr2:61888509-61888693 | Common:1; Rare:79 |