| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:39035282-39035455 | Rare:40; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:39052043-39052345 | Common:2; Rare:53 | ||||
| chr2:39052385-39052576 | Rare:29 | ||||
| chr2:39091561-39091838 | Common:2; Rare:65 | ||||
| chr2:39112373-39112474 | Rare:19 | ||||
| chr2:39112720-39112778 | Rare:9 | ||||
| chr2:39113976-39114278 | Common:2; Rare:75 | ||||
| chr2:39119760-39119835 | Rare:27 | ||||
| chr2:39290747-39290963 | Common:2; Rare:50 | ||||
| chr2:39435089-39435345 | Common:4; Rare:57 | ||||
| chr2:39435374-39435651 | Common:1; Rare:63 | ||||
| chr2:39479631-39479864 | Common:1; Rare:49 | ||||
| chr2:39516574-39516874 | Common:2; Rare:55 | ||||
| chr2:41157572-41157871 | Common:1; Rare:75 | ||||
| chr2:42256612-42256650 | Rare:8 |