| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202265668-202265791 | Rare:43 | ||||
| chr2:202377261-202377372 | Rare:22 | ||||
| chr2:202912127-202912298 | Common:2; Rare:57 | ||||
| chr2:202912474-202912554 | Common:2; Rare:26 | ||||
| chr2:203014696-203014952 | Common:1; Rare:77 | ||||
| chr2:203238794-203239044 | Rare:91 | ||||
| chr2:203239226-203239320 | Rare:31 | ||||
| chr2:203328130-203328416 | Common:2; Rare:106 | ||||
| chr2:203535175-203535546 | Common:3; Rare:147 | ||||
| chr2:205682356-205682578 | Rare:40 | ||||
| chr2:206085824-206085964 | Common:1; Rare:38 | ||||
| chr2:206086073-206086209 | Rare:19 | ||||
| chr2:206159379-206159683 | Common:3; Rare:100; Clinvar (benign):1 | ||||
| chr2:206274938-206275041 | Rare:40 | ||||
| chr2:206765288-206765621 | Common:2; Rare:84; Clinvar:4; Clinvar (benign):1 |