Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40449898-40450169 | Common:4; Rare:101 | ||||
chr1:40508679-40508793 | Common:3; Rare:32 | ||||
chr1:40531497-40531717 | Rare:60 | ||||
chr1:40691460-40691852 | Common:3; Rare:174 | ||||
chr1:40692033-40692165 | Rare:51 | ||||
chr1:40709191-40709377 | Rare:47 | ||||
chr1:41242104-41242358 | Rare:74 | ||||
chr1:42335157-42335346 | Common:3; Rare:100 | ||||
chr1:42658275-42658558 | Common:3; Rare:79 | ||||
chr1:42682606-42682731 | Common:1; Rare:52 | ||||
chr1:42766562-42766722 | Rare:40; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42766976-42767303 | Common:4; Rare:110; Clinvar (benign):1 | ||||
chr1:42846392-42846638 | Common:1; Rare:68 | ||||
chr1:42958805-42959078 | Common:4; Rare:74; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43171911-43172157 | Rare:76 |