| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:233854509-233854775 | Common:4; Rare:71 | ||||
| chr2:234951817-234952162 | Common:1; Rare:89 | ||||
| chr2:236569612-236569884 | Common:8; Rare:49 | ||||
| chr2:237085815-237085955 | Common:1; Rare:58 | ||||
| chr2:237487011-237487283 | Common:4; Rare:58 | ||||
| chr2:238060741-238061022 | Common:4; Rare:86 | ||||
| chr2:238203616-238203821 | Common:3; Rare:89 | ||||
| chr2:240025263-240025480 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136264-240136442 | Common:1; Rare:80 | ||||
| chr2:241102270-241102357 | Common:2; Rare:35 | ||||
| chr2:241255097-241255582 | Common:1; Rare:109 | ||||
| chr2:241271945-241272051 | Common:1; Rare:25 | ||||
| chr2:241272789-241272907 | Rare:43 | ||||
| chr2:241315114-241315398 | Common:5; Rare:97 | ||||
| chr2:241315633-241315989 | Common:5; Rare:137 |