| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9555671-9555992 | Common:2; Rare:108 | ||||
| chr2:9843250-9843556 | Common:6; Rare:92 | ||||
| chr2:10689934-10690006 | Common:2; Rare:22 | ||||
| chr2:11746517-11746641 | Common:1; Rare:39; Clinvar:2 | ||||
| chr2:15561300-15561427 | Rare:51 | ||||
| chr2:17753711-17754183 | Common:4; Rare:146; Clinvar (benign):1 | ||||
| chr2:18560685-18560853 | Rare:55 | ||||
| chr2:19901652-19901764 | Common:1; Rare:58 | ||||
| chr2:19901941-19902019 | Common:1; Rare:21 | ||||
| chr2:19990046-19990229 | Rare:51 | ||||
| chr2:20651042-20651223 | Rare:50 | ||||
| chr2:23940379-23940514 | Common:3; Rare:49 | ||||
| chr2:24047346-24047613 | Common:1; Rare:66 | ||||
| chr2:24076413-24076751 | Common:1; Rare:66 | ||||
| chr2:24123262-24123506 | Common:1; Rare:65 |