| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9003957-9004087 | Rare:55 | ||||
| chr2:9423157-9423265 | Common:1; Rare:24 | ||||
| chr2:9423393-9423794 | Rare:125 | ||||
| chr2:9555609-9555958 | Common:2; Rare:118 | ||||
| chr2:9630949-9631344 | Common:3; Rare:126 | ||||
| chr2:9843245-9843544 | Common:6; Rare:90 | ||||
| chr2:10122594-10122814 | Common:5; Rare:97 | ||||
| chr2:10689910-10690029 | Common:2; Rare:40 | ||||
| chr2:11746499-11746655 | Common:1; Rare:47; Clinvar:2 | ||||
| chr2:15561284-15561380 | Rare:46 | ||||
| chr2:17518344-17518650 | Common:3; Rare:108 | ||||
| chr2:17753721-17754174 | Common:4; Rare:143; Clinvar (benign):1 | ||||
| chr2:18560678-18560801 | Rare:30 | ||||
| chr2:19901642-19901756 | Common:1; Rare:58 | ||||
| chr2:19901948-19902037 | Common:1; Rare:27 |