Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:39927561-39927745 | Common:1; Rare:55 | ||||
chr17:40318085-40318283 | Common:1; Rare:43 | ||||
chr17:41688676-41688894 | Common:1; Rare:75 | ||||
chr17:41812836-41813022 | Rare:49; Clinvar:2 | ||||
chr17:41919000-41919306 | Common:2; Rare:91 | ||||
chr17:41966606-41966802 | Common:1; Rare:69 | ||||
chr17:42017640-42017797 | Rare:35 | ||||
chr17:42154934-42155265 | Common:3; Rare:89 | ||||
chr17:42423171-42423462 | Common:1; Rare:74; Clinvar:1 | ||||
chr17:42577671-42577824 | Rare:71 | ||||
chr17:42833371-42833479 | Rare:43 | ||||
chr17:42964429-42964534 | Rare:50 | ||||
chr17:43125354-43125642 | Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170191-43170394 | Rare:46 | ||||
chr17:43171043-43171236 | Rare:56 |