Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44186713-44187034 | Rare:100 | ||||
chr17:44324791-44324980 | Common:2; Rare:65 | ||||
chr17:44503383-44503472 | Rare:37 | ||||
chr17:44899387-44899468 | Rare:32 | ||||
chr17:45060935-45061339 | Common:3; Rare:102 | ||||
chr17:47649648-47650009 | Common:1; Rare:135 | ||||
chr17:47831462-47831680 | Rare:71 | ||||
chr17:47941380-47941600 | Rare:46; Clinvar:1 | ||||
chr17:48048071-48048363 | Rare:69 | ||||
chr17:48048599-48048813 | Common:4; Rare:31 | ||||
chr17:48544579-48544699 | Rare:66 | ||||
chr17:48544711-48544801 | Common:2; Rare:25 | ||||
chr17:48944783-48944918 | Common:2; Rare:39 | ||||
chr17:49788593-49788697 | Rare:29 | ||||
chr17:50192477-50192663 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):3 |