Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43171043-43171245 | Rare:61 | ||||
chr17:44070570-44070935 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186691-44187002 | Rare:104 | ||||
chr17:44503377-44503727 | Rare:135 | ||||
chr17:44899375-44899736 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
chr17:44947700-44947930 | Common:1; Rare:67 | ||||
chr17:45051582-45051691 | Rare:37 | ||||
chr17:45060987-45061341 | Common:2; Rare:95 | ||||
chr17:45148192-45148476 | Common:1; Rare:88 | ||||
chr17:47941374-47941702 | Rare:89; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48048061-48048384 | Rare:86 | ||||
chr17:48048602-48048812 | Common:4; Rare:29 | ||||
chr17:48610537-48610826 | Common:3; Rare:107 | ||||
chr17:48944783-48944909 | Common:2; Rare:37 | ||||
chr17:48997360-48997527 | Rare:35 |