Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145996534-145996845 | Common:1; Rare:126 | ||||
chr1:147172371-147172797 | Common:1; Rare:115 | ||||
chr1:147541235-147541616 | Common:2; Rare:61 | ||||
chr1:147599627-147599827 | Rare:52 | ||||
chr1:147600095-147600335 | Rare:96 | ||||
chr1:147670416-147670687 | Common:2; Rare:62 | ||||
chr1:147773364-147773462 | Common:2; Rare:27; Clinvar (benign):2 | ||||
chr1:149886668-149886959 | Rare:96 | ||||
chr1:149887961-149888215 | Rare:50 | ||||
chr1:149927734-149927910 | Common:1; Rare:67; Clinvar (benign):5 | ||||
chr1:149928239-149928355 | Rare:22 | ||||
chr1:150010631-150010867 | Common:2; Rare:61 | ||||
chr1:150067115-150067373 | Common:4; Rare:50 | ||||
chr1:150067646-150067894 | Rare:71 | ||||
chr1:150149768-150150281 | Common:3; Rare:188 |