Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37859575-37859798 | Common:3; Rare:73 | ||||
chr1:37989969-37990170 | Rare:73 | ||||
chr1:38873301-38873540 | Common:3; Rare:83 | ||||
chr1:39883478-39883590 | Rare:39 | ||||
chr1:39954983-39955163 | Common:1; Rare:48 | ||||
chr1:40040455-40040812 | Common:3; Rare:110 | ||||
chr1:40097240-40097334 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
chr1:40161277-40161402 | Rare:32 | ||||
chr1:40257908-40258255 | Common:4; Rare:89; Clinvar:6 | ||||
chr1:40450042-40450164 | Common:3; Rare:42 | ||||
chr1:40508662-40508787 | Common:3; Rare:34 | ||||
chr1:40691590-40691833 | Common:1; Rare:116 | ||||
chr1:40692039-40692230 | Common:1; Rare:60 | ||||
chr1:40709154-40709374 | Rare:52 | ||||
chr1:40979627-40979739 | Rare:40 |