Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:45418258-45418591 | Common:1; Rare:90 | ||||
chr13:45464632-45465156 | Common:1; Rare:126 | ||||
chr13:46052696-46052886 | Common:2; Rare:55 | ||||
chr13:46104899-46105270 | Common:3; Rare:91 | ||||
chr13:46797673-46797896 | Common:1; Rare:42 | ||||
chr13:48001253-48001444 | Common:2; Rare:86; Clinvar:3; Clinvar (benign):3 | ||||
chr13:48037671-48037782 | Rare:58 | ||||
chr13:48037920-48038116 | Common:5; Rare:60 | ||||
chr13:48975661-48975934 | Common:2; Rare:86 | ||||
chr13:48976544-48976828 | Common:1; Rare:82 | ||||
chr13:49247830-49247989 | Rare:50 | ||||
chr13:49444002-49444492 | Common:1; Rare:154 | ||||
chr13:49496104-49496297 | Common:4; Rare:54 | ||||
chr13:49585499-49585658 | Common:1; Rare:58 | ||||
chr13:49936222-49936569 | Common:1; Rare:107 |