| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32627937-32628123 | Rare:58 | ||||
| chr2:33476540-33476646 | Common:2; Rare:17 | ||||
| chr2:33599210-33599442 | Common:1; Rare:88 | ||||
| chr2:37084267-37084568 | Common:4; Rare:113 | ||||
| chr2:37231525-37231732 | Common:4; Rare:121; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:37324735-37324922 | Common:1; Rare:77 | ||||
| chr2:37671486-37671773 | Common:2; Rare:110 | ||||
| chr2:37672190-37672262 | Rare:20 | ||||
| chr2:38076137-38076291 | Rare:39 | ||||
| chr2:38602886-38602942 | Rare:26 | ||||
| chr2:38751272-38751568 | Common:4; Rare:156 | ||||
| chr2:38875875-38876059 | Common:2; Rare:68 | ||||
| chr2:39121001-39121141 | Rare:51 | ||||
| chr2:39437077-39437464 | Common:4; Rare:139 | ||||
| chr2:42169170-42169436 | Common:1; Rare:132 |