Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:95233924-95234243 | Common:5; Rare:96 | ||||
chr1:98661587-98661891 | Common:2; Rare:105 | ||||
chr1:99645335-99645768 | Common:1; Rare:72 | ||||
chr1:99645987-99646361 | Rare:74 | ||||
chr1:99766625-99766727 | Rare:21 | ||||
chr1:99849997-99850662 | Common:1; Rare:170; Clinvar:3; Clinvar (benign):2 | ||||
chr1:99969872-99970089 | Rare:48 | ||||
chr1:100038001-100038114 | Common:1; Rare:46 | ||||
chr1:100132911-100133224 | Common:2; Rare:119 | ||||
chr1:100178116-100178352 | Common:2; Rare:34 | ||||
chr1:100249803-100250045 | Common:4; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266089-100266419 | Common:4; Rare:120 | ||||
chr1:100894640-100894923 | Common:2; Rare:67 | ||||
chr1:100895955-100896155 | Rare:56 | ||||
chr1:101025754-101025936 | Common:1; Rare:54 |