Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32769404-32769739 | Rare:85 | ||||
chr1:33347133-33347253 | Rare:19 | ||||
chr1:35434942-35435196 | Common:2; Rare:60 | ||||
chr1:35577738-35577952 | Rare:53 | ||||
chr1:39632945-39633269 | Common:1; Rare:77 | ||||
chr1:39956830-39957181 | Rare:72 | ||||
chr1:39968378-39968630 | Common:2; Rare:59 | ||||
chr1:40064351-40064552 | Rare:47 | ||||
chr1:40385367-40385564 | Common:1; Rare:28 | ||||
chr1:40388580-40388828 | Rare:53 | ||||
chr1:40394902-40394917 | Rare:2 | ||||
chr1:40394957-40394993 | Common:1; Rare:5 | ||||
chr1:41035421-41035514 | Common:2; Rare:24 | ||||
chr1:43272534-43272604 | Rare:9 | ||||
chr1:43439744-43439942 | Rare:61; Clinvar (benign):1 |