| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:150479247-150479396 | Rare:31 | ||||
| chr2:150480292-150480443 | Common:1; Rare:21 | ||||
| chr2:150484362-150484643 | Common:1; Rare:44 | ||||
| chr2:151258155-151258374 | Rare:41 | ||||
| chr2:151420761-151420874 | Common:1; Rare:19 | ||||
| chr2:151424860-151425106 | Common:3; Rare:58 | ||||
| chr2:151434745-151434854 | Common:1; Rare:20 | ||||
| chr2:151495713-151495822 | Common:1; Rare:18 | ||||
| chr2:151502853-151502978 | Common:1; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:151618812-151618988 | Rare:29 | ||||
| chr2:151740942-151741143 | Common:2; Rare:39 | ||||
| chr2:151783081-151783352 | Common:2; Rare:39 | ||||
| chr2:151789974-151790051 | Rare:10 | ||||
| chr2:151797067-151797397 | Common:1; Rare:44 | ||||
| chr2:151806940-151807248 | Rare:55 |