| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237966728-237967039 | Common:3; Rare:91 | ||||
| chr2:238060712-238061057 | Common:4; Rare:110 | ||||
| chr2:238107703-238107832 | Rare:42 | ||||
| chr2:238203616-238203827 | Common:3; Rare:95 | ||||
| chr2:238426672-238427070 | Common:6; Rare:117 | ||||
| chr2:239401641-239401771 | Rare:66 | ||||
| chr2:240025307-240025480 | Rare:68; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:240136274-240136404 | Common:1; Rare:60 | ||||
| chr2:240560756-240560901 | Common:2; Rare:67 | ||||
| chr2:240561059-240561322 | Common:4; Rare:117 | ||||
| chr2:240586258-240586383 | Common:1; Rare:41 | ||||
| chr2:241102280-241102395 | Common:2; Rare:38 | ||||
| chr2:241149434-241149549 | Common:2; Rare:35 | ||||
| chr2:241315146-241315398 | Common:5; Rare:84 | ||||
| chr2:241315649-241316183 | Common:5; Rare:194 |