| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:153477874-153478172 | Common:2; Rare:53 | ||||
| chr2:161430589-161430661 | Rare:11 | ||||
| chr2:161625700-161625853 | Rare:38 | ||||
| chr2:162839502-162839573 | Rare:18 | ||||
| chr2:170770729-170771124 | Common:2; Rare:74 | ||||
| chr2:172083905-172084235 | Common:2; Rare:66 | ||||
| chr2:178413900-178413981 | Rare:28 | ||||
| chr2:182866248-182866391 | Rare:54; Clinvar:1 | ||||
| chr2:186695324-186695371 | Rare:10 | ||||
| chr2:198374531-198374724 | Rare:36 | ||||
| chr2:198544597-198544729 | Rare:16 | ||||
| chr2:199414713-199414747 | Rare:5 | ||||
| chr2:199440654-199440716 | Common:1; Rare:10 | ||||
| chr2:199445294-199445568 | Common:1; Rare:38 | ||||
| chr2:199456910-199457040 | Common:2; Rare:27 |