Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37989961-37990266 | Common:1; Rare:99 | ||||
chr1:38873309-38873554 | Common:3; Rare:84 | ||||
chr1:39026237-39026390 | Common:1; Rare:39 | ||||
chr1:39883480-39883570 | Rare:29 | ||||
chr1:40040437-40040829 | Common:3; Rare:119 | ||||
chr1:40161233-40161399 | Common:1; Rare:45 | ||||
chr1:40257908-40258283 | Common:4; Rare:101; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40508666-40508773 | Common:3; Rare:30 | ||||
chr1:40691470-40691764 | Common:3; Rare:140 | ||||
chr1:40692039-40692206 | Common:1; Rare:56 | ||||
chr1:40979423-40979766 | Common:5; Rare:110 | ||||
chr1:42335199-42335386 | Common:5; Rare:87 | ||||
chr1:42658286-42658473 | Common:2; Rare:54 | ||||
chr1:42767023-42767309 | Common:4; Rare:88 | ||||
chr1:42816995-42817136 | Common:1; Rare:36 |