Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:50346698-50347183 | Common:2; Rare:158; Clinvar:6; Clinvar (benign):14 | ||||
chr2:50347355-50347416 | Common:1; Rare:8 | ||||
chr2:50347502-50347785 | Common:3; Rare:78 | ||||
chr2:50347788-50347970 | Rare:38 | ||||
chr2:50348000-50348056 | Common:1; Rare:13 | ||||
chr2:51032019-51032287 | Common:1; Rare:65; Clinvar:3 | ||||
chr2:51032355-51032601 | Common:7; Rare:59; Clinvar:6 | ||||
chr2:53767739-53767871 | Common:2; Rare:49 | ||||
chr2:53786823-53787220 | Common:1; Rare:149 | ||||
chr2:53970788-53971226 | Common:12; Rare:156 | ||||
chr2:54115421-54115684 | Rare:88 | ||||
chr2:54456006-54456409 | Common:5; Rare:155 | ||||
chr2:54457023-54457396 | Common:3; Rare:138 | ||||
chr2:54558114-54558452 | Common:2; Rare:105 | ||||
chr2:54723391-54723620 | Rare:67 |