| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219245391-219245531 | Rare:40 | ||||
| chr2:219253867-219254054 | Common:1; Rare:58 | ||||
| chr2:219279203-219279545 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr2:219387595-219387635 | Rare:4 | ||||
| chr2:219418504-219419080 | Common:5; Rare:189; Clinvar:38; Clinvar (benign):18; Clinvar (pathogenic):2 | ||||
| chr2:219419845-219420364 | Common:3; Rare:136; Clinvar:14; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
| chr2:219420484-219420953 | Common:2; Rare:128; Clinvar:17; Clinvar (benign):16; Clinvar (pathogenic):4 | ||||
| chr2:219425636-219425788 | Rare:28; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr2:219460595-219460927 | Common:3; Rare:74 | ||||
| chr2:219497905-219498058 | Common:1; Rare:36 | ||||
| chr2:219498663-219498938 | Common:2; Rare:62 | ||||
| chr2:219543816-219544044 | Common:3; Rare:69 | ||||
| chr2:219597734-219597922 | Common:2; Rare:75 | ||||
| chr2:221572266-221572524 | Common:6; Rare:92 | ||||
| chr2:221573954-221574066 | Rare:25 |