Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69801624-69802065 | Common:3; Rare:102 | ||||
chr10:70132807-70132906 | Rare:20 | ||||
chr10:70170448-70170795 | Common:3; Rare:103 | ||||
chr10:70233304-70233667 | Common:6; Rare:120; Clinvar (benign):1 | ||||
chr10:71319156-71319288 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):1 | ||||
chr10:71851187-71851454 | Common:5; Rare:112; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72273695-72273964 | Rare:84 | ||||
chr10:72354893-72355219 | Common:2; Rare:118 | ||||
chr10:72626035-72626266 | Common:1; Rare:56 | ||||
chr10:73111022-73111110 | Common:2; Rare:8 | ||||
chr10:73167933-73168141 | Rare:52 | ||||
chr10:73252387-73252463 | Rare:27; Clinvar (benign):1 | ||||
chr10:73252552-73252808 | Common:2; Rare:75; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73495613-73495772 | Rare:33 | ||||
chr10:73625955-73626118 | Rare:29 |