Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46297042-46297349 | Common:6; Rare:131 | ||||
chr2:46297675-46297801 | Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
chr2:46356557-46356785 | Rare:42 | ||||
chr2:46616991-46617270 | Common:7; Rare:126 | ||||
chr2:46915722-46915923 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
chr2:46916007-46916135 | Common:2; Rare:38 | ||||
chr2:46941645-46941770 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
chr2:47176444-47176574 | Rare:94; Clinvar (benign):5 | ||||
chr2:47402951-47403194 | Common:1; Rare:111; Clinvar:36; Clinvar (benign):26 | ||||
chr2:47782953-47783161 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
chr2:48440619-48440861 | Common:8; Rare:114 | ||||
chr2:53786852-53787213 | Common:1; Rare:138 | ||||
chr2:53970788-53971133 | Common:10; Rare:118 | ||||
chr2:55050428-55050749 | Common:4; Rare:97 | ||||
chr2:55232259-55232726 | Common:3; Rare:130 |