Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39738744-39738930 | Common:2; Rare:48 | ||||
chr1:39883480-39883577 | Rare:33 | ||||
chr1:40040444-40040814 | Common:3; Rare:114 | ||||
chr1:40097234-40097295 | Rare:28; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40161276-40161402 | Rare:32 | ||||
chr1:40257903-40258265 | Common:4; Rare:98; Clinvar:7 | ||||
chr1:40449995-40450175 | Common:3; Rare:69 | ||||
chr1:40508626-40508789 | Common:5; Rare:49 | ||||
chr1:40691385-40691852 | Common:3; Rare:195 | ||||
chr1:40692062-40692230 | Common:1; Rare:50 | ||||
chr1:40979415-40979806 | Common:5; Rare:126 | ||||
chr1:42335175-42335346 | Common:3; Rare:91 | ||||
chr1:42456233-42456583 | Common:1; Rare:106 | ||||
chr1:42456908-42456969 | Rare:22 | ||||
chr1:42658275-42658466 | Common:2; Rare:56 |