| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:28394592-28394789 | Common:1; Rare:73 | ||||
| chr2:28436629-28437020 | Common:4; Rare:196 | ||||
| chr2:28437360-28437905 | Common:1; Rare:165 | ||||
| chr2:28510385-28510541 | Common:2; Rare:27 | ||||
| chr2:28567006-28567545 | Common:11; Rare:244 | ||||
| chr2:28664388-28664788 | Common:18; Rare:147 | ||||
| chr2:28683000-28683410 | Common:2; Rare:67 | ||||
| chr2:28683507-28683683 | Common:1; Rare:29 | ||||
| chr2:28716120-28716610 | Common:2; Rare:75 | ||||
| chr2:28736175-28736362 | Rare:33 | ||||
| chr2:29105866-29106312 | Common:8; Rare:68 | ||||
| chr2:29108336-29108578 | Common:3; Rare:40 | ||||
| chr2:29118958-29119287 | Rare:62 | ||||
| chr2:29127119-29127245 | Common:1; Rare:19 | ||||
| chr2:29233500-29233747 | Common:2; Rare:72; Clinvar:9; Clinvar (benign):4 |