Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:12195841-12196225 | Rare:93 | ||||
chr10:13099966-13100230 | Common:3; Rare:68; Clinvar:3; Clinvar (benign):5 | ||||
chr10:14838040-14838328 | Common:2; Rare:77 | ||||
chr10:18659254-18659530 | Common:2; Rare:94 | ||||
chr10:27154293-27154480 | Rare:49 | ||||
chr10:28533034-28533189 | Rare:61 | ||||
chr10:35127157-35127227 | Rare:14 | ||||
chr10:43138368-43138547 | Common:2; Rare:67 | ||||
chr10:45000906-45000948 | Rare:15 | ||||
chr10:68332895-68332979 | Common:1; Rare:22 | ||||
chr10:71851204-71851452 | Common:5; Rare:107; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72273914-72274102 | Rare:67 | ||||
chr10:73096790-73096869 | Common:2; Rare:26 | ||||
chr10:73167970-73168119 | Rare:36 | ||||
chr10:73744256-73744414 | Common:1; Rare:42 |