Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:47324277-47324460 | Common:4; Rare:45 | ||||
chr17:47530960-47531217 | Rare:64 | ||||
chr17:47531790-47531939 | Common:1; Rare:32 | ||||
chr17:47649217-47649486 | Rare:76 | ||||
chr17:47649596-47650196 | Common:1; Rare:206 | ||||
chr17:47650444-47650895 | Common:4; Rare:174 | ||||
chr17:47733024-47733337 | Common:1; Rare:71 | ||||
chr17:47821674-47821975 | Common:3; Rare:70 | ||||
chr17:47831443-47831715 | Rare:90 | ||||
chr17:47840949-47841490 | Rare:123 | ||||
chr17:47895708-47895855 | Common:3; Rare:38 | ||||
chr17:47896192-47896290 | Rare:36 | ||||
chr17:47896451-47896673 | Common:1; Rare:49 | ||||
chr17:47941261-47941809 | Rare:144; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr17:47970687-47971215 | Common:4; Rare:138 |