| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:19901925-19902010 | Common:1; Rare:23 | ||||
| chr2:19990062-19990229 | Rare:44 | ||||
| chr2:20350815-20351071 | Common:1; Rare:110 | ||||
| chr2:20446849-20447113 | Common:4; Rare:118 | ||||
| chr2:20447278-20447654 | Common:2; Rare:111 | ||||
| chr2:20823056-20823182 | Common:1; Rare:46 | ||||
| chr2:23927063-23927334 | Common:3; Rare:94 | ||||
| chr2:23940379-23940537 | Common:3; Rare:59 | ||||
| chr2:24076225-24076958 | Common:3; Rare:147 | ||||
| chr2:24123255-24123506 | Common:1; Rare:66 | ||||
| chr2:24793073-24793161 | Rare:44 | ||||
| chr2:24971705-24971854 | Common:1; Rare:55 | ||||
| chr2:24971902-24972189 | Common:1; Rare:93 | ||||
| chr2:26033725-26034159 | Common:4; Rare:163 | ||||
| chr2:26194568-26194864 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 |