| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47402904-47403208 | Common:2; Rare:261; Clinvar:85; Clinvar (benign):62; Clinvar (pathogenic):2 | ||||
| chr2:47782946-47783214 | Common:4; Rare:227; Clinvar:12; Clinvar (benign):20 | ||||
| chr2:47905489-47905885 | Common:3; Rare:266 | ||||
| chr2:47906020-47906209 | Common:2; Rare:103 | ||||
| chr2:48314189-48314373 | Common:2; Rare:113 | ||||
| chr2:48314376-48314803 | Rare:299 | ||||
| chr2:48440611-48440865 | Common:15; Rare:227 | ||||
| chr2:53767470-53767929 | Common:10; Rare:271 | ||||
| chr2:53786818-53787241 | Common:2; Rare:314 | ||||
| chr2:53970741-53971182 | Common:23; Rare:305 | ||||
| chr2:54115202-54115490 | Rare:64 | ||||
| chr2:54115537-54115681 | Rare:99 | ||||
| chr2:54115782-54116008 | Common:10; Rare:167 | ||||
| chr2:54456046-54456433 | Common:3; Rare:261 | ||||
| chr2:54456860-54457240 | Common:4; Rare:259 |