Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73625949-73626118 | Rare:30 | ||||
chr10:73744251-73744445 | Common:1; Rare:51 | ||||
chr10:73781977-73782084 | Common:1; Rare:36 | ||||
chr10:73874469-73874723 | Rare:62 | ||||
chr10:73997753-73998374 | Common:2; Rare:158; Clinvar:4; Clinvar (benign):4 | ||||
chr10:74104887-74105250 | Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
chr10:74151038-74151267 | Common:1; Rare:66 | ||||
chr10:75111300-75111738 | Common:1; Rare:122 | ||||
chr10:75210454-75210891 | Common:2; Rare:151 | ||||
chr10:75235328-75235468 | Rare:24 | ||||
chr10:77637416-77637502 | Common:1; Rare:23; Clinvar:3; Clinvar (benign):1 | ||||
chr10:78029466-78029643 | Common:1; Rare:53; Clinvar (benign):1 | ||||
chr10:80078614-80078696 | Rare:30 | ||||
chr10:80079170-80079302 | Common:1; Rare:54 | ||||
chr10:80204331-80204504 | Common:2; Rare:30 |