| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201116689-201116848 | Rare:34 | ||||
| chr2:201118426-201118821 | Rare:62 | ||||
| chr2:201258332-201258382 | Rare:23 | ||||
| chr2:201260380-201260609 | Common:1; Rare:51 | ||||
| chr2:203238931-203239035 | Rare:39 | ||||
| chr2:206085844-206086005 | Common:1; Rare:35 | ||||
| chr2:206159345-206159679 | Common:3; Rare:104; Clinvar (benign):1 | ||||
| chr2:207165929-207166094 | Rare:29 | ||||
| chr2:207529771-207530125 | Common:3; Rare:97 | ||||
| chr2:207624565-207624692 | Rare:31 | ||||
| chr2:208255069-208255226 | Common:2; Rare:43 | ||||
| chr2:210002358-210002645 | Common:6; Rare:89 | ||||
| chr2:216081761-216081925 | Common:1; Rare:58 | ||||
| chr2:216412700-216412773 | Rare:10 | ||||
| chr2:216498721-216498867 | Common:4; Rare:56 |