Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155978369-155978684 | Common:1; Rare:100 | ||||
chr1:155979084-155979263 | Common:1; Rare:31 | ||||
chr1:156020869-156021042 | Rare:55 | ||||
chr1:156054585-156054884 | Common:3; Rare:87 | ||||
chr1:156054922-156055102 | Common:1; Rare:42 | ||||
chr1:156082419-156082661 | Rare:56 | ||||
chr1:156106233-156106314 | Rare:12 | ||||
chr1:156134363-156134969 | Common:2; Rare:142; Clinvar:21; Clinvar (benign):12; Clinvar (pathogenic):14 | ||||
chr1:156135938-156136461 | Common:4; Rare:168; Clinvar:37; Clinvar (benign):22; Clinvar (pathogenic):13 | ||||
chr1:156193817-156194136 | Common:3; Rare:78 | ||||
chr1:156212878-156213141 | Common:1; Rare:92 | ||||
chr1:156282789-156282959 | Common:2; Rare:46 | ||||
chr1:156295530-156295575 | Rare:9 | ||||
chr1:156335826-156336003 | Common:1; Rare:43 | ||||
chr1:156337835-156337882 | Rare:8 |