| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210303540-210303824 | Common:3; Rare:54 | ||||
| chr2:210314917-210315300 | Common:7; Rare:107 | ||||
| chr2:210477572-210477690 | Rare:39 | ||||
| chr2:212539140-212539358 | Common:6; Rare:44 | ||||
| chr2:213151719-213152058 | Common:2; Rare:144 | ||||
| chr2:213152274-213152286 | Rare:3 | ||||
| chr2:213152332-213152381 | Rare:12 | ||||
| chr2:213284210-213284534 | Rare:110 | ||||
| chr2:214809630-214810036 | Common:3; Rare:146; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:215311997-215312145 | Common:7; Rare:64 | ||||
| chr2:215365547-215365928 | Common:6; Rare:95 | ||||
| chr2:215375627-215375952 | Common:2; Rare:83 | ||||
| chr2:215435750-215435903 | Common:1; Rare:35 | ||||
| chr2:215435916-215435964 | Rare:10 | ||||
| chr2:215435971-215436241 | Common:2; Rare:86 |