| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:38751231-38751287 | Rare:26 | ||||
| chr2:38751319-38751551 | Common:3; Rare:116 | ||||
| chr2:38875868-38876075 | Common:2; Rare:76 | ||||
| chr2:39121004-39121108 | Rare:33 | ||||
| chr2:39436940-39437019 | Common:1; Rare:36 | ||||
| chr2:39437082-39437476 | Common:4; Rare:142 | ||||
| chr2:42047754-42048036 | Common:4; Rare:95 | ||||
| chr2:42169292-42169514 | Common:1; Rare:109 | ||||
| chr2:42568414-42568770 | Common:6; Rare:92 | ||||
| chr2:43226550-43226865 | Common:3; Rare:132 | ||||
| chr2:43595924-43596186 | Common:1; Rare:84 | ||||
| chr2:43637116-43637319 | Common:2; Rare:68 | ||||
| chr2:43898944-43899630 | Common:2; Rare:203; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:43995954-43996329 | Common:5; Rare:161; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:44361479-44362007 | Common:3; Rare:165 |