| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202912127-202912304 | Common:2; Rare:58 | ||||
| chr2:202912505-202912584 | Rare:29 | ||||
| chr2:203014494-203014948 | Common:1; Rare:144 | ||||
| chr2:203238836-203239050 | Common:1; Rare:84 | ||||
| chr2:203239229-203239320 | Rare:31 | ||||
| chr2:203328190-203328434 | Common:2; Rare:92 | ||||
| chr2:203533379-203533532 | Rare:26 | ||||
| chr2:203535208-203535546 | Common:3; Rare:138 | ||||
| chr2:205682356-205682508 | Rare:27 | ||||
| chr2:205682668-205682780 | Rare:30 | ||||
| chr2:206085769-206086051 | Common:2; Rare:75 | ||||
| chr2:206086073-206086220 | Rare:19 | ||||
| chr2:206086260-206086303 | Rare:4 | ||||
| chr2:206159370-206159989 | Common:4; Rare:185; Clinvar (benign):1 | ||||
| chr2:206274897-206275057 | Common:1; Rare:54 |