Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:230186095-230186219 | Rare:31 | ||||
chr2:231393687-231393804 | Rare:21 | ||||
chr2:231482884-231482978 | Rare:23 | ||||
chr2:234495922-234496080 | Rare:46 | ||||
chr2:237689518-237689784 | Rare:46 | ||||
chr2:241741199-241741379 | Rare:31 | ||||
chr2:241804756-241804991 | Rare:70 | ||||
chr2:241842972-241842990 | Rare:6 | ||||
chr2:241881275-241881423 | Rare:36 | ||||
chr20:326236-326324 | Common:1; Rare:23 | ||||
chr20:327327-327448 | Rare:51 | ||||
chr20:2837040-2837374 | Rare:58 | ||||
chr20:3082794-3083062 | Common:3; Rare:80; Clinvar (pathogenic):1 | ||||
chr20:3083421-3083669 | Common:2; Rare:57 | ||||
chr20:3083879-3084005 | Rare:22 |