Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:159924564-159924673 | Rare:25 | ||||
chr1:159925457-159925617 | Common:1; Rare:42 | ||||
chr1:160031828-160032060 | Common:2; Rare:62 | ||||
chr1:160262379-160262574 | Rare:57 | ||||
chr1:160285120-160285259 | Common:3; Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
chr1:160343187-160343389 | Rare:83 | ||||
chr1:161021118-161021410 | Rare:70 | ||||
chr1:161038905-161039022 | Common:1; Rare:42 | ||||
chr1:161045878-161046050 | Common:1; Rare:45 | ||||
chr1:161098289-161098391 | Common:1; Rare:16 | ||||
chr1:161118012-161118128 | Rare:51 | ||||
chr1:161132431-161132661 | Common:1; Rare:82 | ||||
chr1:161166257-161166504 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161199051-161199299 | Rare:39 | ||||
chr1:161225768-161226063 | Common:10; Rare:43 |