| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:233854509-233854755 | Common:4; Rare:66 | ||||
| chr2:236567572-236567783 | Common:1; Rare:62 | ||||
| chr2:236569607-236569831 | Common:8; Rare:40 | ||||
| chr2:237085761-237085951 | Common:2; Rare:69 | ||||
| chr2:237334816-237334941 | Common:1; Rare:40; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:237414067-237414400 | Common:2; Rare:67; Clinvar (benign):2 | ||||
| chr2:237487157-237487301 | Common:2; Rare:39 | ||||
| chr2:237966728-237967089 | Common:4; Rare:112 | ||||
| chr2:238060761-238061099 | Common:6; Rare:107 | ||||
| chr2:238203565-238203815 | Common:5; Rare:100 | ||||
| chr2:238426906-238427083 | Common:1; Rare:62 | ||||
| chr2:238847845-238848230 | Common:1; Rare:87 | ||||
| chr2:238848495-238848692 | Rare:40; Clinvar (pathogenic):1 | ||||
| chr2:239401398-239401429 | Rare:14 | ||||
| chr2:239401647-239401750 | Rare:49 |