| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219419858-219420178 | Common:2; Rare:68; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:219437176-219437477 | Common:2; Rare:51 | ||||
| chr2:219441901-219442071 | Rare:37 | ||||
| chr2:219444567-219444741 | Rare:48 | ||||
| chr2:219460592-219460899 | Common:3; Rare:68 | ||||
| chr2:219491606-219491868 | Common:2; Rare:50 | ||||
| chr2:219497553-219497642 | Common:1; Rare:15 | ||||
| chr2:219497812-219498039 | Common:3; Rare:46 | ||||
| chr2:219498663-219498925 | Common:2; Rare:55 | ||||
| chr2:219543724-219544044 | Common:3; Rare:97 | ||||
| chr2:219597688-219598142 | Common:3; Rare:178 | ||||
| chr2:221572254-221572490 | Common:3; Rare:81 | ||||
| chr2:223052072-223052201 | Rare:26 | ||||
| chr2:226799165-226799296 | Common:1; Rare:36 | ||||
| chr2:226799661-226799967 | Rare:97 |