| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:23927208-23927325 | Common:2; Rare:39 | ||||
| chr2:23940379-23940514 | Common:3; Rare:49 | ||||
| chr2:24049592-24049754 | Rare:46 | ||||
| chr2:24076204-24076743 | Common:1; Rare:135 | ||||
| chr2:24123275-24123506 | Common:1; Rare:61 | ||||
| chr2:24793122-24793164 | Rare:22 | ||||
| chr2:24971705-24971882 | Common:2; Rare:70 | ||||
| chr2:24971907-24972136 | Common:1; Rare:75 | ||||
| chr2:25878444-25878742 | Common:3; Rare:88 | ||||
| chr2:26033792-26034151 | Common:3; Rare:128 | ||||
| chr2:26195219-26195356 | Rare:39; Clinvar (benign):1 | ||||
| chr2:26244563-26244972 | Common:2; Rare:152; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345798-26346156 | Common:1; Rare:107 | ||||
| chr2:26764212-26764325 | Rare:43 | ||||
| chr2:27032867-27033004 | Rare:51 |