Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:58046724-58046845 | Rare:38 | ||||
chr2:61017434-61017753 | Common:1; Rare:96; Clinvar:2 | ||||
chr2:61144926-61145165 | Common:3; Rare:79 | ||||
chr2:61177158-61177458 | Common:6; Rare:119 | ||||
chr2:61184527-61184764 | Common:1; Rare:69 | ||||
chr2:61470661-61471034 | Common:1; Rare:122 | ||||
chr2:61471245-61471378 | Common:2; Rare:48 | ||||
chr2:61888575-61888736 | Common:1; Rare:66 | ||||
chr2:63588241-63588546 | Common:1; Rare:89; Clinvar:6 | ||||
chr2:63588624-63589045 | Common:1; Rare:130; Clinvar (benign):1 | ||||
chr2:63840815-63841142 | Common:1; Rare:92 | ||||
chr2:63841593-63841934 | Common:2; Rare:115 | ||||
chr2:64524089-64524436 | Common:3; Rare:110 | ||||
chr2:65056163-65056473 | Common:2; Rare:109 | ||||
chr2:65227579-65227954 | Rare:100 |