Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54801287-54801388 | Rare:18 | ||||
chr1:54886370-54886891 | Common:3; Rare:289 | ||||
chr1:54886994-54887469 | Common:6; Rare:306; Clinvar:10; Clinvar (benign):4 | ||||
chr1:55039353-55039630 | Common:4; Rare:121; Clinvar:7; Clinvar (benign):2 | ||||
chr1:55214450-55215020 | Common:8; Rare:277 | ||||
chr1:55215311-55215559 | Rare:175 | ||||
chr1:56579525-56579677 | Rare:34 | ||||
chr1:56579624-56579729 | Rare:15 | ||||
chr1:56645114-56645379 | Common:2; Rare:141 | ||||
chr1:58699994-58700167 | Common:7; Rare:155 | ||||
chr1:58783977-58784388 | Common:1; Rare:170 | ||||
chr1:59296450-59297128 | Common:27; Rare:294 | ||||
chr1:59511480-59511940 | Common:5; Rare:142 | ||||
chr1:59512070-59512366 | Rare:123 | ||||
chr1:59814491-59815250 | Common:10; Rare:361 |