Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70888530-70888692 | Common:2; Rare:52; Clinvar:5; Clinvar (benign):2 | ||||
chr10:71773490-71773751 | Common:3; Rare:74 | ||||
chr10:71819544-71819801 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):2 | ||||
chr10:71851187-71851431 | Common:5; Rare:104; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72088694-72088761 | Rare:12 | ||||
chr10:72216205-72216340 | Rare:58 | ||||
chr10:72273693-72273953 | Rare:72 | ||||
chr10:72354881-72355211 | Common:2; Rare:118 | ||||
chr10:73096797-73097035 | Common:3; Rare:73 | ||||
chr10:73097082-73097172 | Common:1; Rare:22 | ||||
chr10:73110363-73110522 | Rare:31 | ||||
chr10:73167965-73168353 | Rare:113 | ||||
chr10:73252556-73252829 | Common:2; Rare:80; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73358733-73358897 | Common:2; Rare:42 | ||||
chr10:73413989-73414137 | Common:2; Rare:41 |