Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40709119-40709469 | Rare:84 | ||||
chr1:40783570-40783890 | Common:1; Rare:70 | ||||
chr1:40862292-40862571 | Common:5; Rare:97 | ||||
chr1:40979572-40979799 | Common:3; Rare:84 | ||||
chr1:40979860-40980056 | Rare:69 | ||||
chr1:41242106-41242329 | Rare:67 | ||||
chr1:42334312-42334553 | Rare:73 | ||||
chr1:42335165-42335468 | Common:5; Rare:135 | ||||
chr1:42380623-42380818 | Common:1; Rare:62 | ||||
chr1:42456211-42456634 | Common:2; Rare:136 | ||||
chr1:42462996-42463306 | Common:3; Rare:95 | ||||
chr1:42658258-42658501 | Common:2; Rare:73 | ||||
chr1:42682051-42682426 | Common:2; Rare:114 | ||||
chr1:42682686-42683086 | Common:3; Rare:246 | ||||
chr1:42766967-42767357 | Common:6; Rare:139; Clinvar (benign):1; Clinvar (pathogenic):1 |