Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:165827734-165827829 | Common:1; Rare:28 | ||||
chr1:166839274-166839539 | Rare:84 | ||||
chr1:167094004-167094110 | Rare:21 | ||||
chr1:167220534-167220942 | Common:2; Rare:128 | ||||
chr1:167629971-167630357 | Common:6; Rare:71 | ||||
chr1:167935882-167936261 | Common:1; Rare:104 | ||||
chr1:167936549-167936961 | Common:1; Rare:146 | ||||
chr1:168225918-168226086 | Common:2; Rare:61 | ||||
chr1:169106079-169106399 | Common:5; Rare:112 | ||||
chr1:169107819-169107968 | Common:1; Rare:30 | ||||
chr1:169367739-169368271 | Common:3; Rare:109 | ||||
chr1:169427410-169427509 | Rare:19 | ||||
chr1:169485652-169486219 | Common:2; Rare:167; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169708759-169708879 | Common:2; Rare:35 | ||||
chr1:169794690-169794759 | Rare:12 |