Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:43879492-43879648 | Common:1; Rare:41 | ||||
chr13:43879666-43879913 | Common:18; Rare:67 | ||||
chr13:44989437-44989601 | Rare:62 | ||||
chr13:45120392-45120577 | Common:1; Rare:59 | ||||
chr13:45341040-45341547 | Common:4; Rare:236 | ||||
chr13:45464670-45465015 | Common:1; Rare:86 | ||||
chr13:46052718-46052821 | Common:2; Rare:29 | ||||
chr13:48001253-48001430 | Common:1; Rare:81; Clinvar:3; Clinvar (benign):3 | ||||
chr13:48037954-48038145 | Common:3; Rare:46 | ||||
chr13:48303674-48303887 | Rare:72; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:48976495-48976656 | Common:2; Rare:55 | ||||
chr13:49247807-49247976 | Rare:48 | ||||
chr13:49443996-49444322 | Common:1; Rare:110 | ||||
chr13:49495867-49496055 | Rare:45 | ||||
chr13:49585527-49585658 | Common:1; Rare:47 |