Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:48303563-48304084 | Common:1; Rare:164; Clinvar:16; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr13:48411948-48411997 | Rare:21; Clinvar (pathogenic):1 | ||||
chr13:48492208-48492832 | Common:4; Rare:113 | ||||
chr13:48532409-48533230 | Common:8; Rare:262 | ||||
chr13:48653836-48653992 | Rare:32 | ||||
chr13:48975449-48976301 | Common:2; Rare:236 | ||||
chr13:48976358-48976831 | Common:3; Rare:144 | ||||
chr13:49110201-49110387 | Common:3; Rare:63 | ||||
chr13:49247752-49248144 | Common:1; Rare:105 | ||||
chr13:49443415-49443764 | Rare:50 | ||||
chr13:49443882-49444612 | Common:4; Rare:219 | ||||
chr13:49444645-49444757 | Common:5; Rare:21 | ||||
chr13:49444759-49444897 | Rare:23 | ||||
chr13:49445083-49445226 | Common:1; Rare:31 | ||||
chr13:49495535-49495650 | Rare:25 |