| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201115967-201116454 | Common:2; Rare:89 | ||||
| chr2:201117422-201117601 | Rare:22 | ||||
| chr2:201433472-201433784 | Common:3; Rare:59 | ||||
| chr2:201451379-201451926 | Common:3; Rare:135 | ||||
| chr2:201642641-201642743 | Rare:52 | ||||
| chr2:201780875-201780993 | Common:2; Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202238444-202238632 | Rare:66; Clinvar:1 | ||||
| chr2:202265655-202265834 | Rare:70 | ||||
| chr2:202911569-202911961 | Common:1; Rare:84 | ||||
| chr2:202912141-202912303 | Common:1; Rare:55 | ||||
| chr2:203014636-203014933 | Common:1; Rare:94 | ||||
| chr2:203238719-203239042 | Common:1; Rare:103 | ||||
| chr2:203239220-203239320 | Rare:33 | ||||
| chr2:203328052-203328443 | Common:2; Rare:144 | ||||
| chr2:203535155-203535557 | Common:3; Rare:153 |