Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37808147-37808631 | Common:2; Rare:129 | ||||
chr1:38012524-38012826 | Rare:91 | ||||
chr1:38873312-38873563 | Common:3; Rare:90 | ||||
chr1:39738785-39738913 | Common:1; Rare:29 | ||||
chr1:40161293-40161409 | Rare:29 | ||||
chr1:40257915-40258390 | Common:4; Rare:136; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40508656-40508789 | Common:3; Rare:35 | ||||
chr1:40691586-40691801 | Common:1; Rare:107 | ||||
chr1:40692042-40692203 | Common:1; Rare:53 | ||||
chr1:40979359-40979807 | Common:5; Rare:137 | ||||
chr1:41242117-41242188 | Rare:18 | ||||
chr1:42456265-42456577 | Common:1; Rare:95 | ||||
chr1:42766975-42767309 | Common:4; Rare:113; Clinvar (benign):1 | ||||
chr1:42816927-42817139 | Common:1; Rare:61 | ||||
chr1:42817225-42817458 | Rare:89 |