| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:226836210-226837183 | Common:15; Rare:451 | ||||
| chr2:227164154-227164704 | Rare:313; Clinvar:15 | ||||
| chr2:227297050-227297477 | Common:4; Rare:177 | ||||
| chr2:227325117-227325366 | Common:14; Rare:259 | ||||
| chr2:227325941-227326163 | Rare:61 | ||||
| chr2:227472769-227473114 | Common:6; Rare:119 | ||||
| chr2:229271120-229271460 | Common:2; Rare:99 | ||||
| chr2:229921225-229921625 | Common:7; Rare:181 | ||||
| chr2:229921612-229922853 | Common:13; Rare:902 | ||||
| chr2:230067334-230068460 | Common:18; Rare:344 | ||||
| chr2:230068710-230068945 | Rare:44 | ||||
| chr2:230219904-230220360 | Common:4; Rare:153 | ||||
| chr2:230327068-230327204 | Rare:28 | ||||
| chr2:230341986-230342154 | Common:5; Rare:49 | ||||
| chr2:230342130-230342517 | Common:16; Rare:228 |