| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:132331799-132332298 | Common:16; Rare:166 | ||||
| chr10:132397093-132397227 | Common:3; Rare:22 | ||||
| chr10:132397640-132398120 | Rare:104 | ||||
| chr10:132537265-132538000 | Common:4; Rare:398 | ||||
| chr10:132942870-132943075 | Common:11; Rare:46 | ||||
| chr10:133159842-133160031 | Common:9; Rare:48 | ||||
| chr10:133308820-133308975 | Rare:76 | ||||
| chr10:133309090-133309421 | Common:2; Rare:124 | ||||
| chr10:133358005-133358183 | Common:3; Rare:44 | ||||
| chr10:133373339-133373497 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr10:133378985-133379301 | Common:18; Rare:61 | ||||
| chr10:133394005-133394229 | Common:2; Rare:93 | ||||
| chr10:133520221-133520470 | Common:4; Rare:80 | ||||
| chr11:207352-207770 | Common:9; Rare:137 | ||||
| chr11:208615-208843 | Rare:80 |