Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:134918601-134918857 | Common:1; Rare:100 | ||||
chr2:135052208-135052298 | Common:1; Rare:39; Clinvar (benign):1 | ||||
chr2:135531199-135531502 | Common:1; Rare:52 | ||||
chr2:137964134-137964590 | Common:2; Rare:82 | ||||
chr2:144517331-144517787 | Common:5; Rare:130; Clinvar:3; Clinvar (benign):4 | ||||
chr2:144520312-144520524 | Common:4; Rare:40; Clinvar (benign):1 | ||||
chr2:148020708-148021011 | Common:1; Rare:62 | ||||
chr2:148021563-148021658 | Rare:19 | ||||
chr2:151828482-151828784 | Common:2; Rare:78 | ||||
chr2:152717829-152717947 | Rare:47 | ||||
chr2:152717999-152718261 | Common:1; Rare:80 | ||||
chr2:152718491-152718637 | Rare:55 | ||||
chr2:158968485-158968688 | Rare:64 | ||||
chr2:159615225-159615302 | Common:2; Rare:18 | ||||
chr2:159615524-159615702 | Common:1; Rare:63 |