Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:46387224-46387351 | Rare:32 | ||||
chr13:48001229-48001408 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):6 | ||||
chr13:48037505-48037801 | Common:1; Rare:124; Clinvar:1 | ||||
chr13:48037940-48038052 | Common:4; Rare:31 | ||||
chr13:48233060-48233475 | Common:3; Rare:144 | ||||
chr13:48303692-48303914 | Rare:67; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:48975830-48975928 | Rare:36 | ||||
chr13:48976435-48976662 | Common:3; Rare:80 | ||||
chr13:49247830-49247998 | Rare:53 | ||||
chr13:49443997-49444517 | Common:2; Rare:162 | ||||
chr13:49585479-49585624 | Common:1; Rare:47 | ||||
chr13:49936231-49936592 | Common:1; Rare:112 | ||||
chr13:49996785-49997099 | Common:1; Rare:61 | ||||
chr13:50081969-50082299 | Common:1; Rare:92 | ||||
chr13:50715514-50715646 | Rare:27 |