| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36355469-36356009 | Common:3; Rare:192 | ||||
| chr2:36356483-36356622 | Rare:62 | ||||
| chr2:37076143-37076282 | Common:6; Rare:26 | ||||
| chr2:37084267-37084557 | Common:4; Rare:107 | ||||
| chr2:37231472-37231685 | Common:5; Rare:106; Clinvar (benign):3 | ||||
| chr2:37344569-37344690 | Rare:44 | ||||
| chr2:37671423-37671745 | Common:1; Rare:111 | ||||
| chr2:38602624-38602681 | Rare:23 | ||||
| chr2:38751220-38751362 | Common:2; Rare:89 | ||||
| chr2:38875868-38876105 | Common:2; Rare:84 | ||||
| chr2:39120998-39121345 | Common:2; Rare:113 | ||||
| chr2:39436976-39437486 | Common:5; Rare:194 | ||||
| chr2:42054995-42055329 | Common:2; Rare:95 | ||||
| chr2:42359867-42359936 | Rare:15 | ||||
| chr2:42568415-42568770 | Common:6; Rare:92 |