| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237966769-237967089 | Common:4; Rare:99 | ||||
| chr2:238060706-238061057 | Common:4; Rare:112 | ||||
| chr2:238203583-238203821 | Common:3; Rare:101 | ||||
| chr2:238426880-238427067 | Common:1; Rare:69 | ||||
| chr2:240025276-240025480 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136243-240136382 | Rare:55 | ||||
| chr2:240560756-240560898 | Common:2; Rare:66 | ||||
| chr2:241102270-241102372 | Common:2; Rare:39 | ||||
| chr2:241149425-241149600 | Common:2; Rare:58 | ||||
| chr2:241272789-241272947 | Rare:65 | ||||
| chr2:241315156-241315408 | Common:4; Rare:80 | ||||
| chr2:241315641-241316009 | Common:5; Rare:140 | ||||
| chr2:241508530-241508867 | Common:2; Rare:105 | ||||
| chr2:241637506-241637704 | Common:1; Rare:108 | ||||
| chr2:241686692-241686973 | Rare:96 |