| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201118432-201118868 | Rare:139 | ||||
| chr2:201118890-201119420 | Common:1; Rare:112 | ||||
| chr2:201233306-201233570 | Common:2; Rare:86 | ||||
| chr2:201257793-201258118 | Common:1; Rare:54 | ||||
| chr2:201258163-201258758 | Common:6; Rare:199; Clinvar (benign):3 | ||||
| chr2:201451300-201451842 | Common:5; Rare:352 | ||||
| chr2:201629376-201630029 | Common:2; Rare:202; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr2:201642608-201642971 | Common:2; Rare:266; Clinvar (benign):2 | ||||
| chr2:201643380-201643810 | Common:4; Rare:134; Clinvar:7; Clinvar (benign):4 | ||||
| chr2:201780755-201781380 | Common:9; Rare:371; Clinvar:9; Clinvar (benign):6 | ||||
| chr2:202034035-202034238 | Common:2; Rare:123 | ||||
| chr2:202034903-202035532 | Common:1; Rare:225 | ||||
| chr2:202238466-202238723 | Common:1; Rare:201; Clinvar:1 | ||||
| chr2:202265600-202266033 | Common:2; Rare:300 | ||||
| chr2:202375953-202376709 | Common:4; Rare:232; Clinvar:3; Clinvar (benign):3 |