Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:46617025-46617252 | Common:6; Rare:89 | ||||
chr2:46699003-46699331 | Common:1; Rare:99 | ||||
chr2:47782971-47783189 | Common:2; Rare:94; Clinvar:3; Clinvar (benign):5 | ||||
chr2:53786906-53787145 | Rare:90 | ||||
chr2:54115510-54115642 | Rare:39 | ||||
chr2:61144907-61145128 | Common:2; Rare:68 | ||||
chr2:63841593-63841896 | Common:2; Rare:102 | ||||
chr2:68157509-68157949 | Common:2; Rare:226 | ||||
chr2:71068539-71068672 | Rare:59 | ||||
chr2:71130227-71130321 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
chr2:74147876-74148140 | Common:1; Rare:62; Clinvar:2 | ||||
chr2:74421582-74421759 | Rare:62 | ||||
chr2:74483029-74483093 | Rare:27 | ||||
chr2:74529680-74530009 | Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74958872-74959024 | Rare:58 |