| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202238443-202238625 | Rare:63; Clinvar:1 | ||||
| chr2:202265675-202265791 | Rare:42 | ||||
| chr2:202377045-202377367 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:202912154-202912298 | Common:1; Rare:49 | ||||
| chr2:202912507-202912554 | Rare:16 | ||||
| chr2:203014672-203014925 | Common:1; Rare:73 | ||||
| chr2:203238945-203239051 | Common:1; Rare:41 | ||||
| chr2:203239240-203239326 | Rare:30 | ||||
| chr2:203328150-203328423 | Common:2; Rare:102 | ||||
| chr2:206085772-206085960 | Common:1; Rare:54 | ||||
| chr2:206086281-206086417 | Rare:24 | ||||
| chr2:206159345-206159989 | Common:4; Rare:188; Clinvar (benign):1 | ||||
| chr2:206765276-206765654 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166142 | Rare:42 | ||||
| chr2:207529710-207530025 | Common:3; Rare:104 |