Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:167630113-167630326 | Common:3; Rare:38 | ||||
chr1:167721751-167722022 | Common:4; Rare:77 | ||||
chr1:167935904-167936329 | Common:2; Rare:120 | ||||
chr1:167936546-167936750 | Common:1; Rare:67 | ||||
chr1:167936869-167936953 | Rare:32 | ||||
chr1:168178835-168179102 | Common:4; Rare:96 | ||||
chr1:168225720-168226072 | Common:4; Rare:112 | ||||
chr1:169367784-169368246 | Common:3; Rare:84 | ||||
chr1:169485654-169486169 | Common:1; Rare:154; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794868-169795074 | Common:3; Rare:47 | ||||
chr1:170074461-170074771 | Common:3; Rare:91 | ||||
chr1:170531989-170532202 | Common:1; Rare:86; Clinvar:1 | ||||
chr1:170663029-170663197 | Rare:42 | ||||
chr1:171485344-171485598 | Rare:91 | ||||
chr1:171741910-171742122 | Common:2; Rare:66 |