| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219245373-219245531 | Rare:46 | ||||
| chr2:219253861-219254056 | Common:1; Rare:61 | ||||
| chr2:219279232-219279545 | Common:3; Rare:100; Clinvar (benign):1 | ||||
| chr2:219419858-219420155 | Common:2; Rare:62; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:219498663-219498938 | Common:2; Rare:62 | ||||
| chr2:219505986-219506299 | Common:1; Rare:101; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:219543802-219544083 | Common:3; Rare:87 | ||||
| chr2:219571530-219571605 | Rare:16 | ||||
| chr2:219597737-219597909 | Common:1; Rare:70 | ||||
| chr2:221572266-221572528 | Common:6; Rare:94 | ||||
| chr2:221573960-221574037 | Rare:19 | ||||
| chr2:223052098-223052197 | Rare:21 | ||||
| chr2:223837518-223837852 | Common:1; Rare:74 | ||||
| chr2:223837904-223837907 | Rare:1 | ||||
| chr2:223837936-223837970 | Common:1; Rare:10 |