| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:31233890-31234156 | Common:1; Rare:72 | ||||
| chr2:32010529-32010804 | Rare:69 | ||||
| chr2:32010959-32011166 | Rare:61 | ||||
| chr2:32039740-32039948 | Rare:66 | ||||
| chr2:32063305-32063714 | Common:2; Rare:139; Clinvar:1 | ||||
| chr2:32063858-32064017 | Common:1; Rare:84; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:32165653-32165924 | Common:1; Rare:111 | ||||
| chr2:32277770-32277924 | Common:1; Rare:33 | ||||
| chr2:32356656-32357255 | Common:7; Rare:214 | ||||
| chr2:32627886-32628053 | Rare:42 | ||||
| chr2:32946850-32947169 | Common:4; Rare:105 | ||||
| chr2:33599164-33599640 | Common:1; Rare:168 | ||||
| chr2:36355469-36355782 | Common:2; Rare:114 | ||||
| chr2:36356225-36357009 | Common:4; Rare:447 | ||||
| chr2:36597520-36597940 | Common:5; Rare:167 |