| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200864548-200864807 | Common:1; Rare:94 | ||||
| chr2:200887939-200887981 | Rare:8 | ||||
| chr2:200888568-200888862 | Rare:68 | ||||
| chr2:200888941-200889479 | Common:3; Rare:169 | ||||
| chr2:200963165-200963337 | Rare:33 | ||||
| chr2:200963438-200963890 | Common:1; Rare:113 | ||||
| chr2:201071592-201072058 | Rare:102 | ||||
| chr2:201116263-201116467 | Rare:39 | ||||
| chr2:201117409-201117596 | Rare:23 | ||||
| chr2:201118607-201118863 | Rare:38 | ||||
| chr2:201183008-201183167 | Common:1; Rare:24; Clinvar (benign):2 | ||||
| chr2:201233369-201233585 | Common:1; Rare:37 | ||||
| chr2:201233701-201233965 | Rare:46 | ||||
| chr2:201257975-201258248 | Common:2; Rare:55; Clinvar (benign):1 | ||||
| chr2:201258280-201258373 | Rare:38 |