| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38602895-38603087 | Common:3; Rare:82 | ||||
| chr2:38751342-38751628 | Common:4; Rare:132 | ||||
| chr2:38875868-38876089 | Common:2; Rare:79 | ||||
| chr2:39437303-39437453 | Common:2; Rare:52 | ||||
| chr2:40511992-40512018 | Rare:5 | ||||
| chr2:40512368-40512720 | Common:3; Rare:71 | ||||
| chr2:42792502-42792862 | Common:3; Rare:112 | ||||
| chr2:43595957-43596203 | Common:1; Rare:89 | ||||
| chr2:43676413-43676482 | Rare:17 | ||||
| chr2:44361485-44362005 | Common:3; Rare:163 | ||||
| chr2:46617019-46617276 | Common:7; Rare:112 | ||||
| chr2:46915724-46916135 | Common:4; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176430-47176618 | Rare:126; Clinvar (benign):5 | ||||
| chr2:47345045-47345143 | Rare:24 | ||||
| chr2:47369263-47369533 | Common:2; Rare:112; Clinvar:8; Clinvar (benign):3 |