Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39955584-39955978 | Common:1; Rare:90 | ||||
chr1:40039671-40040499 | Common:5; Rare:198 | ||||
chr1:40040507-40040896 | Common:3; Rare:117 | ||||
chr1:40041263-40041344 | Rare:16 | ||||
chr1:40096777-40096851 | Common:3; Rare:13 | ||||
chr1:40096852-40097387 | Common:3; Rare:153; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):6 | ||||
chr1:40161157-40161480 | Common:1; Rare:108 | ||||
chr1:40161569-40161857 | Common:1; Rare:71 | ||||
chr1:40257585-40258307 | Common:6; Rare:178; Clinvar:9; Clinvar (benign):1 | ||||
chr1:40258362-40258392 | Rare:5 | ||||
chr1:40315370-40315461 | Rare:20 | ||||
chr1:40373510-40373812 | Common:1; Rare:73 | ||||
chr1:40374300-40374913 | Common:13; Rare:113 | ||||
chr1:40449878-40450228 | Common:5; Rare:126 | ||||
chr1:40450239-40450585 | Common:4; Rare:79 |