Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40140145-40140678 | Common:6; Rare:241 | ||||
chr17:40342038-40342377 | Common:1; Rare:76 | ||||
chr17:41528281-41528550 | Common:1; Rare:60; Clinvar:1 | ||||
chr17:41812621-41813021 | Common:3; Rare:89; Clinvar:5 | ||||
chr17:42017149-42017483 | Rare:109 | ||||
chr17:42017577-42017657 | Rare:28 | ||||
chr17:42154946-42155270 | Common:4; Rare:83 | ||||
chr17:42422802-42423457 | Common:2; Rare:205; Clinvar:5 | ||||
chr17:42458738-42458945 | Common:3; Rare:79 | ||||
chr17:42567001-42567159 | Common:3; Rare:51 | ||||
chr17:42577682-42577844 | Rare:77 | ||||
chr17:42609330-42609742 | Common:8; Rare:173; Clinvar (benign):2 | ||||
chr17:42761046-42761270 | Rare:61 | ||||
chr17:42798677-42798785 | Rare:32 | ||||
chr17:42833385-42833475 | Rare:39 |