Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74465343-74465455 | Common:1; Rare:31; Clinvar:1 | ||||
chr2:74482905-74483119 | Common:1; Rare:76 | ||||
chr2:74507643-74507789 | Rare:36 | ||||
chr2:74529653-74530009 | Rare:110; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74654103-74654367 | Common:1; Rare:90 | ||||
chr2:74833816-74834147 | Common:1; Rare:100 | ||||
chr2:74835272-74835294 | Rare:6 | ||||
chr2:74958876-74959003 | Rare:51 | ||||
chr2:75560875-75561050 | Rare:36 | ||||
chr2:75561258-75561417 | Common:2; Rare:20 | ||||
chr2:75710598-75710743 | Common:1; Rare:51 | ||||
chr2:84459226-84459572 | Common:3; Rare:89; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:84905517-84905953 | Common:1; Rare:132 | ||||
chr2:84906997-84907240 | Common:1; Rare:43 | ||||
chr2:85327916-85328069 | Common:2; Rare:69 |