Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:47782920-47783189 | Common:2; Rare:116; Clinvar:3; Clinvar (benign):5 | ||||
chr2:48440621-48440824 | Common:6; Rare:89 | ||||
chr2:53767496-53767800 | Common:4; Rare:92 | ||||
chr2:53786842-53787090 | Rare:88 | ||||
chr2:53970780-53971177 | Common:12; Rare:145 | ||||
chr2:54723339-54723628 | Common:2; Rare:90 | ||||
chr2:55010217-55010366 | Rare:34 | ||||
chr2:55050493-55050763 | Common:3; Rare:82 | ||||
chr2:55232335-55232726 | Common:2; Rare:113 | ||||
chr2:55269201-55269333 | Common:2; Rare:38 | ||||
chr2:55519452-55519741 | Common:1; Rare:77 | ||||
chr2:58046617-58046875 | Common:2; Rare:81 | ||||
chr2:58241306-58241417 | Rare:65; Clinvar:5; Clinvar (benign):1 | ||||
chr2:60550894-60551025 | Rare:35 | ||||
chr2:60756080-60756296 | Rare:72 |