Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:63588484-63589025 | Common:1; Rare:158; Clinvar:1; Clinvar (benign):1 | ||||
chr2:63840822-63841165 | Common:2; Rare:94 | ||||
chr2:63841614-63841927 | Common:2; Rare:106 | ||||
chr2:64454048-64454247 | Rare:37 | ||||
chr2:64454880-64454896 | Rare:4 | ||||
chr2:64524063-64524422 | Common:3; Rare:109 | ||||
chr2:65056172-65056467 | Common:2; Rare:103 | ||||
chr2:65227603-65227888 | Rare:83 | ||||
chr2:66434829-66435179 | Common:1; Rare:80 | ||||
chr2:68157515-68157957 | Common:2; Rare:227 | ||||
chr2:68252497-68252828 | Common:3; Rare:105 | ||||
chr2:68467292-68467688 | Common:1; Rare:107 | ||||
chr2:69387183-69387377 | Rare:50; Clinvar:2 | ||||
chr2:69643616-69643839 | Rare:82 | ||||
chr2:69741788-69742174 | Common:3; Rare:77 |