| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:15561290-15561415 | Rare:51 | ||||
| chr2:17753686-17754174 | Common:5; Rare:151; Clinvar (benign):1 | ||||
| chr2:19901667-19901759 | Common:1; Rare:46 | ||||
| chr2:19901957-19902085 | Common:1; Rare:43 | ||||
| chr2:19990046-19990211 | Rare:45 | ||||
| chr2:20051470-20051836 | Common:1; Rare:109 | ||||
| chr2:20446887-20447091 | Common:2; Rare:74 | ||||
| chr2:20651037-20651236 | Rare:56 | ||||
| chr2:20823055-20823182 | Common:1; Rare:47 | ||||
| chr2:23927073-23927295 | Common:3; Rare:80 | ||||
| chr2:23940379-23940527 | Common:3; Rare:55 | ||||
| chr2:24047351-24047426 | Rare:14 | ||||
| chr2:24076205-24076591 | Rare:105 | ||||
| chr2:24123279-24123506 | Common:1; Rare:60 | ||||
| chr2:24793018-24793181 | Rare:72 |