Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:33993029-33993293 | Common:1; Rare:70 | ||||
chr20:33993766-33994126 | Common:1; Rare:129 | ||||
chr20:34112102-34112437 | Rare:111 | ||||
chr20:34302958-34303399 | Common:2; Rare:171; Clinvar:3; Clinvar (benign):3 | ||||
chr20:34516273-34516455 | Common:3; Rare:76 | ||||
chr20:34558474-34558822 | Common:1; Rare:98 | ||||
chr20:34677051-34677350 | Rare:81 | ||||
chr20:34704124-34704428 | Common:2; Rare:92 | ||||
chr20:34825470-34825789 | Rare:113 | ||||
chr20:34872815-34872976 | Rare:58 | ||||
chr20:34876239-34876624 | Common:3; Rare:103 | ||||
chr20:34955699-34955874 | Common:1; Rare:65; Clinvar:3; Clinvar (benign):3 | ||||
chr20:35092730-35092931 | Common:2; Rare:98 | ||||
chr20:35147280-35147368 | Common:1; Rare:32 | ||||
chr20:35278032-35278321 | Common:7; Rare:100 |