Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:172905013-172905238 | Common:1; Rare:41 | ||||
chr5:173328412-173328605 | Rare:36 | ||||
chr5:176361761-176361928 | Common:2; Rare:43 | ||||
chr5:176388563-176388811 | Common:4; Rare:97 | ||||
chr5:177022626-177022732 | Rare:37 | ||||
chr5:177133465-177133804 | Rare:123 | ||||
chr5:177516932-177517068 | Rare:48; Clinvar (pathogenic):1 | ||||
chr5:179623658-179623970 | Common:4; Rare:102 | ||||
chr5:181261123-181261213 | Rare:23 | ||||
chr6:292414-292537 | Rare:36 | ||||
chr6:2999675-2999912 | Common:10; Rare:47 | ||||
chr6:3118602-3118737 | Common:2; Rare:43 | ||||
chr6:4021165-4021415 | Rare:106 | ||||
chr6:7541390-7541744 | Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
chr6:10415072-10415190 | Common:1; Rare:41 |