Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42798643-42798785 | Rare:46 | ||||
chr17:42833348-42833456 | Rare:40 | ||||
chr17:42964436-42964520 | Rare:43 | ||||
chr17:43125354-43125654 | Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43171030-43171274 | Common:1; Rare:80 | ||||
chr17:43211773-43211906 | Common:1; Rare:29 | ||||
chr17:44070619-44070911 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44170537-44170714 | Rare:33 | ||||
chr17:44186644-44187230 | Common:1; Rare:184 | ||||
chr17:44221211-44221353 | Rare:42 | ||||
chr17:44268089-44268365 | Rare:57; Clinvar:3 | ||||
chr17:44324765-44324987 | Common:2; Rare:80 | ||||
chr17:44503345-44503688 | Rare:140 | ||||
chr17:44899393-44899736 | Common:2; Rare:102; Clinvar:1; Clinvar (benign):1 | ||||
chr17:45060958-45061332 | Common:3; Rare:96 |