| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:132397044-132397286 | Common:3; Rare:52 | ||||
| chr10:132397468-132397714 | Common:1; Rare:62 | ||||
| chr10:132537190-132537397 | Common:2; Rare:80 | ||||
| chr10:132537490-132537910 | Common:2; Rare:136 | ||||
| chr10:133308196-133308456 | Common:3; Rare:56 | ||||
| chr10:133308742-133309181 | Common:2; Rare:170 | ||||
| chr10:133357621-133357882 | Common:2; Rare:43 | ||||
| chr10:133357888-133358035 | Common:2; Rare:45 | ||||
| chr10:133373299-133373553 | Common:2; Rare:107; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr10:133373668-133373815 | Common:1; Rare:50 | ||||
| chr10:133393959-133394335 | Common:2; Rare:162 | ||||
| chr10:133394410-133394509 | Common:1; Rare:34 | ||||
| chr10:133394547-133394636 | Rare:26 | ||||
| chr11:207300-207790 | Common:9; Rare:154 | ||||
| chr11:207911-207967 | Rare:15 |