Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:130342679-130342931 | Common:3; Rare:83 | ||||
chr2:130836832-130836951 | Common:2; Rare:56 | ||||
chr2:131105253-131105356 | Common:1; Rare:47 | ||||
chr2:131492754-131493097 | Common:8; Rare:103 | ||||
chr2:134918591-134918908 | Common:1; Rare:134 | ||||
chr2:135531172-135531508 | Common:1; Rare:70 | ||||
chr2:135985404-135985884 | Common:5; Rare:175; Clinvar (benign):1 | ||||
chr2:138501681-138502011 | Common:2; Rare:110 | ||||
chr2:148020686-148021035 | Common:2; Rare:72; Clinvar (benign):1 | ||||
chr2:150485376-150485511 | Rare:32 | ||||
chr2:152717821-152717942 | Rare:48 | ||||
chr2:152717984-152718296 | Common:1; Rare:102 | ||||
chr2:152718491-152718643 | Rare:57 | ||||
chr2:159615556-159615671 | Common:1; Rare:38 | ||||
chr2:159712390-159712600 | Common:2; Rare:85 |