Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9716857-9717624 | Common:10; Rare:220; Clinvar:2; Clinvar (benign):4 | ||||
chr1:9717655-9717891 | Rare:85 | ||||
chr1:9726525-9726957 | Common:4; Rare:204; Clinvar:1; Clinvar (benign):1 | ||||
chr1:9730745-9731145 | Common:8; Rare:125 | ||||
chr1:9786733-9787240 | Common:4; Rare:157 | ||||
chr1:9787248-9788028 | Common:16; Rare:213 | ||||
chr1:9825658-9825920 | Rare:54 | ||||
chr1:9850120-9850560 | Common:3; Rare:72 | ||||
chr1:9880756-9880977 | Common:1; Rare:47 | ||||
chr1:9900400-9900627 | Rare:70 | ||||
chr1:9911104-9911238 | Rare:17 | ||||
chr1:9950405-9950576 | Common:1; Rare:35 | ||||
chr1:9960817-9960936 | Common:1; Rare:35 | ||||
chr1:9961230-9961620 | Common:3; Rare:111 | ||||
chr1:10018820-10019350 | Common:2; Rare:76 |