Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:39289732-39289992 | Common:2; Rare:52 | ||||
chr17:39509194-39509498 | Common:4; Rare:56 | ||||
chr17:39994966-39995291 | Common:1; Rare:95 | ||||
chr17:40274592-40274859 | Rare:43 | ||||
chr17:40388326-40388580 | Common:1; Rare:40 | ||||
chr17:40413270-40413517 | Common:1; Rare:43 | ||||
chr17:40416260-40416458 | Rare:34; Clinvar (benign):1 | ||||
chr17:40416492-40416793 | Rare:41 | ||||
chr17:40469823-40469959 | Rare:21 | ||||
chr17:40549481-40549618 | Common:1; Rare:23 | ||||
chr17:40552782-40552967 | Common:3; Rare:32 | ||||
chr17:40559637-40559735 | Rare:22 | ||||
chr17:41868562-41869051 | Common:7; Rare:107 | ||||
chr17:42050581-42050778 | Common:1; Rare:47 | ||||
chr17:42275685-42275791 | Rare:22 |