| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:133356930-133357510 | Common:8; Rare:270 | ||||
| chr10:133357610-133357890 | Common:5; Rare:105 | ||||
| chr10:133357900-133358300 | Common:17; Rare:299 | ||||
| chr10:133373211-133373611 | Common:5; Rare:378; Clinvar:3; Clinvar (benign):11; Clinvar (pathogenic):7 | ||||
| chr10:133378944-133379360 | Common:74; Rare:262 | ||||
| chr10:133379370-133379790 | Common:2; Rare:99 | ||||
| chr10:133390044-133390444 | Common:2; Rare:77 | ||||
| chr10:133393780-133394960 | Common:13; Rare:938 | ||||
| chr10:133520131-133520531 | Common:6; Rare:152 | ||||
| chr11:207314-208234 | Common:62; Rare:1086 | ||||
| chr11:208490-209192 | Common:5; Rare:705 | ||||
| chr11:236224-236635 | Common:55; Rare:647 | ||||
| chr11:236680-237190 | Common:18; Rare:651 | ||||
| chr11:237434-237834 | Common:4; Rare:153 | ||||
| chr11:277470-277880 | Rare:51 |