| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219279003-219279436 | Common:2; Rare:119 | ||||
| chr2:219387313-219387435 | Common:1; Rare:27 | ||||
| chr2:219388284-219388561 | Common:1; Rare:43 | ||||
| chr2:219498663-219498943 | Common:2; Rare:63 | ||||
| chr2:219543713-219544108 | Common:3; Rare:123 | ||||
| chr2:219552294-219552453 | Rare:47 | ||||
| chr2:219559046-219559144 | Rare:10 | ||||
| chr2:219571195-219571620 | Common:5; Rare:128; Clinvar:6; Clinvar (benign):3 | ||||
| chr2:219597737-219597892 | Common:1; Rare:55 | ||||
| chr2:219598048-219598258 | Common:1; Rare:69 | ||||
| chr2:221572252-221572478 | Common:3; Rare:78 | ||||
| chr2:222656039-222656484 | Common:3; Rare:142 | ||||
| chr2:222860716-222861082 | Common:4; Rare:127 | ||||
| chr2:223837514-223837699 | Common:1; Rare:48 | ||||
| chr2:223945152-223945399 | Rare:106 |