| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9481121-9481445 | Common:1; Rare:90 | ||||
| chr2:9555615-9555977 | Common:2; Rare:121 | ||||
| chr2:9630950-9631316 | Common:3; Rare:118 | ||||
| chr2:10043318-10043672 | Common:4; Rare:143; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:10689910-10690029 | Common:2; Rare:40 | ||||
| chr2:11465855-11465993 | Rare:42 | ||||
| chr2:11466088-11466126 | Common:2; Rare:16 | ||||
| chr2:11746374-11746655 | Common:1; Rare:75; Clinvar:2 | ||||
| chr2:12716594-12717069 | Common:4; Rare:151 | ||||
| chr2:17753721-17753874 | Common:1; Rare:57 | ||||
| chr2:17754054-17754159 | Common:1; Rare:32; Clinvar (benign):1 | ||||
| chr2:18560643-18560800 | Rare:46 | ||||
| chr2:19358520-19358758 | Common:1; Rare:57 | ||||
| chr2:19901944-19902085 | Common:2; Rare:47 | ||||
| chr2:19990034-19990217 | Rare:51 |