| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47402947-47403197 | Common:1; Rare:117; Clinvar:39; Clinvar (benign):27 | ||||
| chr2:47905502-47905867 | Common:3; Rare:179 | ||||
| chr2:48440619-48440833 | Common:6; Rare:96 | ||||
| chr2:51032014-51032297 | Common:1; Rare:67; Clinvar:3 | ||||
| chr2:51032353-51032596 | Common:7; Rare:60; Clinvar:6 | ||||
| chr2:51032598-51032684 | Rare:24 | ||||
| chr2:53767559-53767839 | Common:4; Rare:96 | ||||
| chr2:53786842-53787169 | Common:1; Rare:122 | ||||
| chr2:53970788-53971218 | Common:12; Rare:154 | ||||
| chr2:54115517-54115693 | Rare:65 | ||||
| chr2:54115892-54115993 | Common:2; Rare:38 | ||||
| chr2:54330800-54330919 | Common:2; Rare:39 | ||||
| chr2:55010200-55010311 | Rare:27 | ||||
| chr2:55050302-55050383 | Rare:36 | ||||
| chr2:55050441-55050904 | Common:7; Rare:138 |