Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:135382-135540 | Rare:40 | ||||
chr10:1048865-1049092 | Common:2; Rare:118 | ||||
chr10:7787964-7788240 | Common:1; Rare:110 | ||||
chr10:7818364-7818512 | Common:1; Rare:33 | ||||
chr10:12195819-12196261 | Rare:124 | ||||
chr10:13300049-13300147 | Rare:36; Clinvar:1 | ||||
chr10:14838053-14838337 | Common:2; Rare:76 | ||||
chr10:14878627-14878884 | Common:2; Rare:78 | ||||
chr10:14954068-14954209 | Rare:38 | ||||
chr10:15860499-15860614 | Rare:27 | ||||
chr10:17643884-17644203 | Common:1; Rare:95 | ||||
chr10:27154334-27154486 | Rare:43 | ||||
chr10:27155227-27155390 | Common:3; Rare:58; Clinvar:2; Clinvar (benign):3 | ||||
chr10:32958149-32958525 | Common:2; Rare:140 | ||||
chr10:42782691-42782829 | Rare:36 |