Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:31234001-31234160 | Rare:42 | ||||
chr2:32039761-32039851 | Rare:27 | ||||
chr2:32165737-32165902 | Common:1; Rare:64 | ||||
chr2:32627889-32628125 | Rare:65 | ||||
chr2:33599242-33599593 | Common:1; Rare:123 | ||||
chr2:37084304-37084561 | Common:3; Rare:98 | ||||
chr2:37231542-37231717 | Common:4; Rare:101; Clinvar (benign):3 | ||||
chr2:37324707-37324950 | Common:1; Rare:97 | ||||
chr2:37344569-37344726 | Common:1; Rare:60 | ||||
chr2:38076138-38076282 | Rare:35 | ||||
chr2:38875897-38876055 | Common:1; Rare:57 | ||||
chr2:39437086-39437469 | Common:4; Rare:138 | ||||
chr2:43595967-43596207 | Common:1; Rare:85 | ||||
chr2:44361775-44362005 | Common:1; Rare:67 | ||||
chr2:46541746-46541817 | Rare:10 |