Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:131105245-131105351 | Common:1; Rare:49 | ||||
chr2:131493034-131493089 | Common:1; Rare:13 | ||||
chr2:134918706-134918877 | Rare:71 | ||||
chr2:135052206-135052309 | Common:1; Rare:42; Clinvar (benign):1 | ||||
chr2:135531177-135531502 | Common:1; Rare:64 | ||||
chr2:135985413-135985705 | Common:4; Rare:127; Clinvar (benign):1 | ||||
chr2:148020728-148021035 | Common:1; Rare:55; Clinvar (benign):1 | ||||
chr2:148021544-148021652 | Rare:21 | ||||
chr2:149587320-149587490 | Common:1; Rare:36 | ||||
chr2:149587675-149587803 | Common:1; Rare:38; Clinvar:1 | ||||
chr2:150487138-150487272 | Common:5; Rare:35 | ||||
chr2:152717829-152717964 | Rare:56 | ||||
chr2:152717999-152718041 | Rare:11 | ||||
chr2:152718485-152718637 | Rare:59 | ||||
chr2:156436151-156436455 | Common:3; Rare:94 |