Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69494712-69494912 | Common:1; Rare:43 | ||||
chr10:70132754-70132908 | Rare:42 | ||||
chr10:70146183-70146321 | Common:2; Rare:53 | ||||
chr10:70146638-70146991 | Common:2; Rare:82 | ||||
chr10:70170449-70170550 | Common:2; Rare:30 | ||||
chr10:70233314-70233550 | Common:6; Rare:87; Clinvar (benign):1 | ||||
chr10:70478709-70478984 | Rare:93 | ||||
chr10:70815806-70816002 | Rare:75 | ||||
chr10:71773499-71773651 | Common:2; Rare:48 | ||||
chr10:71819539-71819879 | Common:1; Rare:138; Clinvar:3; Clinvar (benign):3 | ||||
chr10:72216232-72216528 | Common:3; Rare:90 | ||||
chr10:72273712-72273953 | Rare:67 | ||||
chr10:73096804-73097028 | Common:3; Rare:69 | ||||
chr10:73167964-73168344 | Rare:110 | ||||
chr10:73252594-73252802 | Rare:56; Clinvar:4 |