Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44674313-44674784 | Common:3; Rare:139 | ||||
chr1:44739546-44739937 | Common:3; Rare:145 | ||||
chr1:44740042-44740097 | Rare:18 | ||||
chr1:44740212-44740308 | Rare:12 | ||||
chr1:44740428-44740511 | Rare:11 | ||||
chr1:44775004-44775081 | Rare:15 | ||||
chr1:44775398-44775865 | Common:4; Rare:172 | ||||
chr1:44775880-44775929 | Common:1; Rare:17 | ||||
chr1:44775998-44776116 | Rare:30 | ||||
chr1:44799795-44800048 | Common:3; Rare:48 | ||||
chr1:44800078-44800538 | Common:2; Rare:118 | ||||
chr1:44807757-44808036 | Common:1; Rare:67 | ||||
chr1:44813786-44813987 | Common:1; Rare:51 | ||||
chr1:44986265-44986358 | Rare:8 | ||||
chr1:44986463-44986830 | Common:3; Rare:79; Clinvar:1; Clinvar (benign):1 |