Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44899375-44899741 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
chr17:45051439-45051688 | Common:1; Rare:86 | ||||
chr17:45060992-45061453 | Common:2; Rare:137 | ||||
chr17:45132322-45132656 | Common:3; Rare:98 | ||||
chr17:45148170-45148623 | Common:1; Rare:160 | ||||
chr17:45161494-45161916 | Common:1; Rare:113 | ||||
chr17:46193309-46193600 | Common:5; Rare:81 | ||||
chr17:46922858-46923204 | Common:5; Rare:104; Clinvar:3; Clinvar (benign):8 | ||||
chr17:47323850-47323992 | Common:2; Rare:50 | ||||
chr17:47649420-47649668 | Common:1; Rare:69 | ||||
chr17:47650005-47650284 | Rare:86 | ||||
chr17:47831495-47831582 | Rare:32 | ||||
chr17:47941348-47941768 | Rare:110; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48048048-48048405 | Rare:98 | ||||
chr17:48048643-48048862 | Common:3; Rare:33 |