Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:32350026-32350179 | Rare:79 | ||||
chr17:34255377-34255674 | Common:1; Rare:63 | ||||
chr17:35242900-35243138 | Rare:83 | ||||
chr17:36534803-36535005 | Common:3; Rare:86 | ||||
chr17:37406831-37406927 | Rare:31 | ||||
chr17:39200005-39200347 | Common:2; Rare:106 | ||||
chr17:39688021-39688097 | Rare:23 | ||||
chr17:40015149-40015440 | Common:1; Rare:59 | ||||
chr17:40121837-40121992 | Common:2; Rare:61 | ||||
chr17:41528290-41528678 | Common:2; Rare:81; Clinvar:1 | ||||
chr17:41688815-41689051 | Common:2; Rare:115 | ||||
chr17:41689055-41689069 | Rare:4 | ||||
chr17:41812601-41813010 | Common:3; Rare:86; Clinvar:5 | ||||
chr17:42577681-42577804 | Rare:58 | ||||
chr17:42609291-42609693 | Common:9; Rare:169; Clinvar (benign):1 |