Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42816597-42816721 | Rare:25 | ||||
chr1:42816932-42817136 | Common:1; Rare:56 | ||||
chr1:42817194-42817455 | Rare:93 | ||||
chr1:42846387-42846642 | Common:1; Rare:75 | ||||
chr1:42958823-42959066 | Common:3; Rare:69; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43172207-43172359 | Common:1; Rare:69 | ||||
chr1:43358662-43359128 | Common:7; Rare:140 | ||||
chr1:43360551-43360849 | Common:1; Rare:82 | ||||
chr1:43367961-43368212 | Rare:67 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 | ||||
chr1:43649875-43650173 | Rare:71 | ||||
chr1:43707332-43707544 | Common:2; Rare:63 | ||||
chr1:43946582-43946974 | Rare:104 | ||||
chr1:43969794-43970018 | Rare:55 | ||||
chr1:43974788-43975056 | Common:3; Rare:72 |