Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:12792077-12792195 | Rare:31 | ||||
chr19:12792231-12792738 | Common:3; Rare:113 | ||||
chr19:12792740-12792851 | Rare:27 | ||||
chr19:12801739-12802164 | Common:1; Rare:131 | ||||
chr19:12949174-12949321 | Rare:49 | ||||
chr19:13012079-13012192 | Rare:29 | ||||
chr19:13150216-13150475 | Common:2; Rare:88 | ||||
chr19:13764466-13764577 | Common:1; Rare:45 | ||||
chr19:13906080-13906355 | Rare:57 | ||||
chr19:14136882-14137201 | Common:2; Rare:61 | ||||
chr19:14419283-14419649 | Common:1; Rare:85 | ||||
chr19:14529242-14529690 | Common:1; Rare:190 | ||||
chr19:15049408-15049645 | Common:3; Rare:46 | ||||
chr19:15049670-15049917 | Common:13; Rare:63 | ||||
chr19:15055168-15055531 | Common:3; Rare:108; Clinvar (pathogenic):1 |