| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219387316-219387435 | Common:1; Rare:25 | ||||
| chr2:219441904-219442065 | Rare:37 | ||||
| chr2:219497922-219498067 | Common:1; Rare:33 | ||||
| chr2:219498663-219498928 | Common:2; Rare:56 | ||||
| chr2:219543772-219544097 | Common:3; Rare:104 | ||||
| chr2:219552288-219552545 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chr2:219571535-219571794 | Rare:48 | ||||
| chr2:219597737-219597884 | Common:1; Rare:50 | ||||
| chr2:221572266-221572442 | Common:1; Rare:67 | ||||
| chr2:222656042-222656458 | Common:3; Rare:137 | ||||
| chr2:222671394-222671658 | Common:1; Rare:76 | ||||
| chr2:223052090-223052191 | Rare:21 | ||||
| chr2:223837557-223837907 | Common:2; Rare:84 | ||||
| chr2:223945242-223945360 | Rare:65 | ||||
| chr2:223957248-223957473 | Common:4; Rare:86 |