Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:36442762-36443087 | Common:2; Rare:111 | ||||
chr6:36594172-36594372 | Common:3; Rare:76 | ||||
chr6:36874785-36874870 | Rare:33 | ||||
chr6:36885767-36886011 | Common:3; Rare:80 | ||||
chr6:38639854-38639992 | Rare:39 | ||||
chr6:41053032-41053372 | Common:4; Rare:56 | ||||
chr6:41921104-41921244 | Rare:38 | ||||
chr6:42564172-42564192 | Rare:6 | ||||
chr6:42746069-42746331 | Rare:74 | ||||
chr6:42929209-42929556 | Common:4; Rare:97 | ||||
chr6:42984284-42984609 | Rare:80 | ||||
chr6:43013908-43014344 | Common:1; Rare:89 | ||||
chr6:43053694-43054008 | Common:2; Rare:117; Clinvar:5; Clinvar (benign):1 | ||||
chr6:43516853-43517115 | Common:5; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
chr6:43575963-43576186 | Rare:86; Clinvar:4 |