| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47783842-47784035 | Common:6; Rare:42 | ||||
| chr2:47784105-47784225 | Common:2; Rare:34 | ||||
| chr2:47905489-47905835 | Common:3; Rare:168 | ||||
| chr2:48314175-48315046 | Common:2; Rare:325 | ||||
| chr2:48440609-48440956 | Common:8; Rare:153 | ||||
| chr2:48617724-48617895 | Common:3; Rare:58 | ||||
| chr2:48755667-48755787 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chr2:49154441-49154655 | Common:6; Rare:45; Clinvar (benign):2 | ||||
| chr2:51222135-51222329 | Rare:50 | ||||
| chr2:51225520-51225584 | Rare:13 | ||||
| chr2:53767482-53767891 | Common:5; Rare:135 | ||||
| chr2:53786833-53787218 | Common:1; Rare:147 | ||||
| chr2:53970744-53971313 | Common:14; Rare:202 | ||||
| chr2:54115127-54115710 | Common:1; Rare:160 | ||||
| chr2:54256189-54256299 | Common:1; Rare:33 |