Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:14878637-14878882 | Common:2; Rare:73 | ||||
chr10:14953977-14954209 | Rare:80; Clinvar (benign):1 | ||||
chr10:15097306-15097393 | Common:1; Rare:41 | ||||
chr10:17228481-17228675 | Common:1; Rare:55 | ||||
chr10:17228833-17229026 | Common:3; Rare:49 | ||||
chr10:17230248-17230454 | Common:1; Rare:45 | ||||
chr10:17643898-17644278 | Common:2; Rare:112 | ||||
chr10:17809304-17809486 | Rare:40 | ||||
chr10:18651522-18651666 | Common:1; Rare:51 | ||||
chr10:18659250-18659371 | Common:1; Rare:43 | ||||
chr10:19815957-19816653 | Common:8; Rare:167 | ||||
chr10:21533964-21534330 | Common:3; Rare:153 | ||||
chr10:22714407-22714747 | Rare:136 | ||||
chr10:24722713-24722878 | Common:1; Rare:45 | ||||
chr10:26438060-26438412 | Common:2; Rare:81 |