Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:24722926-24723034 | Rare:31 | ||||
chr10:24723110-24723480 | Common:2; Rare:97 | ||||
chr10:24723903-24724044 | Common:2; Rare:30 | ||||
chr10:25016010-25016187 | Rare:42 | ||||
chr10:25016422-25016723 | Common:9; Rare:121 | ||||
chr10:25016965-25017144 | Common:4; Rare:78 | ||||
chr10:26697376-26697712 | Common:4; Rare:94; Clinvar (benign):1 | ||||
chr10:26697780-26698060 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
chr10:26734236-26734470 | Common:1; Rare:40 | ||||
chr10:26859809-26860953 | Common:6; Rare:371 | ||||
chr10:27100395-27100667 | Common:4; Rare:72; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27153637-27154054 | Common:4; Rare:127 | ||||
chr10:27154331-27154521 | Rare:57 | ||||
chr10:27155099-27155439 | Common:7; Rare:127; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240483-27240659 | Common:2; Rare:58 |