Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71819441-71819902 | Common:2; Rare:186; Clinvar:5; Clinvar (benign):5 | ||||
chr10:71851181-71851464 | Common:5; Rare:120; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216208-72216539 | Common:3; Rare:100 | ||||
chr10:72273652-72274023 | Rare:108 | ||||
chr10:72336664-72336952 | Common:1; Rare:73 | ||||
chr10:72354875-72355033 | Common:2; Rare:77 | ||||
chr10:72355104-72355296 | Rare:43 | ||||
chr10:73096785-73097147 | Common:4; Rare:102 | ||||
chr10:73110171-73110465 | Rare:50 | ||||
chr10:73110473-73110541 | Rare:17 | ||||
chr10:73167951-73168142 | Rare:49 | ||||
chr10:73252565-73252791 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):2 | ||||
chr10:73358736-73358859 | Common:2; Rare:28 | ||||
chr10:73495540-73495771 | Rare:51 | ||||
chr10:73625951-73626118 | Rare:30 |