| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:241272570-241272740 | Common:2; Rare:111 | ||||
| chr2:241272761-241273030 | Rare:129 | ||||
| chr2:241315085-241315473 | Common:12; Rare:256 | ||||
| chr2:241315633-241316189 | Common:10; Rare:354 | ||||
| chr2:241356067-241356361 | Common:4; Rare:116 | ||||
| chr2:241508467-241508916 | Common:4; Rare:257 | ||||
| chr2:241636966-241637724 | Common:6; Rare:626 | ||||
| chr2:241686673-241687150 | Common:9; Rare:299 | ||||
| chr2:241687170-241687510 | Common:6; Rare:117 | ||||
| chr2:241701240-241701580 | Common:10; Rare:147 | ||||
| chr2:241701851-241702090 | Common:2; Rare:177 | ||||
| chr2:241734472-241734738 | Common:12; Rare:198; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:241735290-241735950 | Common:9; Rare:301; Clinvar:6; Clinvar (benign):5 | ||||
| chr2:241808697-241808825 | Common:1; Rare:70 | ||||
| chr2:241808958-241809252 | Common:10; Rare:183 |