| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:19990058-19990209 | Rare:38 | ||||
| chr2:20446866-20447074 | Common:3; Rare:76 | ||||
| chr2:20651054-20651271 | Rare:68 | ||||
| chr2:20823056-20823159 | Rare:41 | ||||
| chr2:23940379-23940518 | Common:3; Rare:51 | ||||
| chr2:24049601-24049743 | Rare:38 | ||||
| chr2:24123267-24123506 | Common:1; Rare:62 | ||||
| chr2:24793073-24793175 | Rare:52 | ||||
| chr2:26244557-26244965 | Common:2; Rare:149; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345798-26346165 | Common:1; Rare:110 | ||||
| chr2:26764210-26764350 | Common:1; Rare:53 | ||||
| chr2:27032841-27033011 | Rare:69 | ||||
| chr2:27071324-27071858 | Common:2; Rare:165 | ||||
| chr2:27211775-27212115 | Common:3; Rare:118 | ||||
| chr2:27212241-27212379 | Common:1; Rare:71 |