Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:53786933-53787170 | Common:1; Rare:99 | ||||
chr2:53970788-53971126 | Common:10; Rare:113 | ||||
chr2:55050494-55050763 | Common:3; Rare:82 | ||||
chr2:55519466-55519741 | Common:1; Rare:72 | ||||
chr2:61144926-61145165 | Common:3; Rare:79 | ||||
chr2:63588987-63589019 | Rare:10 | ||||
chr2:63840822-63841165 | Common:2; Rare:94 | ||||
chr2:63841614-63841921 | Common:2; Rare:103 | ||||
chr2:65227582-65227856 | Rare:72 | ||||
chr2:68157515-68157937 | Common:2; Rare:218 | ||||
chr2:68467277-68467626 | Common:1; Rare:93 | ||||
chr2:69387207-69387398 | Rare:53; Clinvar:2 | ||||
chr2:69829458-69829729 | Rare:110 | ||||
chr2:70086971-70087116 | Rare:66 | ||||
chr2:71130224-71130327 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):2 |