Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40161231-40161399 | Common:1; Rare:46 | ||||
chr1:40257880-40258282 | Common:4; Rare:110; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40508679-40508789 | Common:3; Rare:30 | ||||
chr1:40979600-40979758 | Common:3; Rare:56 | ||||
chr1:41242112-41242327 | Rare:66 | ||||
chr1:42335175-42335310 | Common:1; Rare:65 | ||||
chr1:42456219-42456583 | Common:1; Rare:110 | ||||
chr1:42658324-42658456 | Rare:41 | ||||
chr1:42682143-42682432 | Common:2; Rare:77 | ||||
chr1:42767029-42767309 | Common:3; Rare:81 | ||||
chr1:42846401-42846638 | Common:1; Rare:65 | ||||
chr1:42958857-42959078 | Common:2; Rare:60; Clinvar:5; Clinvar (benign):2 | ||||
chr1:43172207-43172353 | Common:1; Rare:68 | ||||
chr1:43358674-43359123 | Common:7; Rare:133 | ||||
chr1:43367957-43368190 | Rare:60 |