| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219278241-219278361 | Rare:23 | ||||
| chr2:219279203-219279573 | Common:3; Rare:111; Clinvar (benign):1 | ||||
| chr2:219498691-219498938 | Common:2; Rare:56 | ||||
| chr2:219597688-219597936 | Common:2; Rare:102 | ||||
| chr2:221572294-221572522 | Common:6; Rare:76 | ||||
| chr2:222656062-222656429 | Common:3; Rare:112 | ||||
| chr2:223945260-223945425 | Rare:83 | ||||
| chr2:223957248-223957504 | Common:4; Rare:100; Clinvar (benign):1 | ||||
| chr2:224585362-224585517 | Common:3; Rare:70 | ||||
| chr2:224585519-224585849 | Common:2; Rare:74 | ||||
| chr2:224982267-224982518 | Rare:38 | ||||
| chr2:226835902-226836149 | Common:1; Rare:98 | ||||
| chr2:226836332-226836438 | Common:2; Rare:26 | ||||
| chr2:226906531-226906740 | Common:3; Rare:43 | ||||
| chr2:227164140-227164395 | Rare:63; Clinvar:2 |