| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219279203-219279871 | Common:4; Rare:198; Clinvar (benign):4 | ||||
| chr2:219498691-219498938 | Common:2; Rare:56 | ||||
| chr2:219543580-219543911 | Common:1; Rare:109 | ||||
| chr2:219597655-219597884 | Common:1; Rare:81 | ||||
| chr2:222656052-222656453 | Common:3; Rare:129 | ||||
| chr2:223957256-223957475 | Common:4; Rare:81 | ||||
| chr2:226795674-226795979 | Common:2; Rare:97; Clinvar:1 | ||||
| chr2:226835347-226835633 | Common:1; Rare:89 | ||||
| chr2:226835918-226836126 | Common:1; Rare:83 | ||||
| chr2:227164199-227164322 | Rare:34; Clinvar:2 | ||||
| chr2:227325182-227325425 | Common:5; Rare:87 | ||||
| chr2:227717985-227718136 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:229921889-229922210 | Common:3; Rare:121 | ||||
| chr2:229922213-229922513 | Common:1; Rare:92 | ||||
| chr2:230219917-230220018 | Rare:15 |