Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73246813-73247043 | Common:1; Rare:91 | ||||
chr10:73247207-73247411 | Rare:115 | ||||
chr10:73379874-73380140 | Rare:82 | ||||
chr10:73495165-73495321 | Common:1; Rare:39 | ||||
chr10:73730452-73730606 | Common:1; Rare:40 | ||||
chr10:73737514-73737712 | Rare:31 | ||||
chr10:73913656-73914110 | Common:3; Rare:126; Clinvar (benign):5 | ||||
chr10:73915219-73915286 | Rare:22 | ||||
chr10:74090731-74090963 | Common:3; Rare:44 | ||||
chr10:74598570-74598717 | Rare:27 | ||||
chr10:75028179-75028449 | Rare:44 | ||||
chr10:75157172-75157342 | Common:1; Rare:37 | ||||
chr10:75230779-75230927 | Common:1; Rare:37 | ||||
chr10:75232068-75232070 | |||||
chr10:78037043-78037231 | Common:3; Rare:50; Clinvar:1; Clinvar (pathogenic):1 |