Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:43899310-43899522 | Rare:63 | ||||
chr2:44361544-44361873 | Common:2; Rare:98 | ||||
chr2:45567965-45568136 | Common:3; Rare:36 | ||||
chr2:46543278-46543396 | Rare:27 | ||||
chr2:46616976-46617257 | Common:6; Rare:119 | ||||
chr2:46698967-46699314 | Common:1; Rare:113 | ||||
chr2:46915738-46915898 | Common:1; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
chr2:46941155-46941279 | Common:1; Rare:53 | ||||
chr2:46941665-46941884 | Common:4; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
chr2:47176408-47176534 | Rare:88; Clinvar (benign):5 | ||||
chr2:47782883-47783188 | Common:3; Rare:129; Clinvar:3; Clinvar (benign):4 | ||||
chr2:47810962-47811190 | Rare:67 | ||||
chr2:47905491-47905907 | Common:3; Rare:196 | ||||
chr2:48314711-48314778 | Rare:19 | ||||
chr2:48440619-48440798 | Common:6; Rare:72 |