Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38427614-38427725 | Common:1; Rare:26 | ||||
chr1:39104486-39104799 | Common:1; Rare:47 | ||||
chr1:39107502-39107706 | Common:1; Rare:39 | ||||
chr1:39410200-39410211 | Rare:3 | ||||
chr1:39447528-39447841 | Common:1; Rare:76 | ||||
chr1:39567824-39567866 | Rare:11 | ||||
chr1:39976804-39976979 | Common:3; Rare:40 | ||||
chr1:40861102-40861222 | Common:1; Rare:28 | ||||
chr1:42676488-42676542 | Rare:5 | ||||
chr1:42698064-42698151 | Common:1; Rare:16 | ||||
chr1:42924280-42924460 | Common:1; Rare:55 | ||||
chr1:43349015-43349261 | Common:2; Rare:81; Clinvar (benign):1 | ||||
chr1:43595854-43595879 | Rare:2 | ||||
chr1:43985397-43985455 | Common:10; Rare:43 | ||||
chr1:44030300-44030444 | Rare:57 |