Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:47402984-47403180 | Common:1; Rare:88; Clinvar:28; Clinvar (benign):21 | ||||
chr2:47782946-47783185 | Common:2; Rare:101; Clinvar:3; Clinvar (benign):3 | ||||
chr2:47905496-47905712 | Common:3; Rare:106 | ||||
chr2:48440631-48440837 | Common:5; Rare:97 | ||||
chr2:53767559-53767839 | Common:4; Rare:96 | ||||
chr2:53786842-53787184 | Common:1; Rare:130 | ||||
chr2:53970780-53971177 | Common:12; Rare:145 | ||||
chr2:55050431-55050784 | Common:4; Rare:107 | ||||
chr2:58046620-58046845 | Rare:68 | ||||
chr2:58047214-58047447 | Rare:72 | ||||
chr2:60756080-60756294 | Rare:71 | ||||
chr2:60881389-60881664 | Common:2; Rare:97 | ||||
chr2:61017098-61017127 | Rare:8 | ||||
chr2:61017425-61017756 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
chr2:61144901-61145165 | Common:3; Rare:90 |