| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39437100-39437470 | Common:4; Rare:131 | ||||
| chr2:43226368-43226862 | Common:4; Rare:203 | ||||
| chr2:44361775-44362002 | Common:1; Rare:66 | ||||
| chr2:46429042-46429235 | Common:1; Rare:77 | ||||
| chr2:46542559-46542757 | Rare:68 | ||||
| chr2:46616974-46617255 | Common:6; Rare:118 | ||||
| chr2:46915723-46915869 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:53786931-53787098 | Rare:68 | ||||
| chr2:53970770-53971152 | Common:11; Rare:140 | ||||
| chr2:54457054-54457259 | Rare:87 | ||||
| chr2:55050235-55050747 | Common:5; Rare:166 | ||||
| chr2:55232256-55232741 | Common:3; Rare:137 | ||||
| chr2:61017168-61017407 | Common:4; Rare:67 | ||||
| chr2:61017428-61017756 | Common:1; Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61177208-61177536 | Common:5; Rare:139 |