| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:264561-265005 | Common:4; Rare:173 | ||||
| chr2:3379621-3379734 | Common:1; Rare:37 | ||||
| chr2:3519488-3519663 | Common:2; Rare:51 | ||||
| chr2:3558230-3558574 | Common:6; Rare:136 | ||||
| chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423169-9423325 | Common:1; Rare:36 | ||||
| chr2:9423424-9423686 | Rare:79 | ||||
| chr2:9555635-9555905 | Common:2; Rare:87 | ||||
| chr2:9843251-9843512 | Common:6; Rare:73 | ||||
| chr2:10302719-10302993 | Common:5; Rare:83 | ||||
| chr2:10448297-10448702 | Common:1; Rare:125 | ||||
| chr2:10689940-10690002 | Common:1; Rare:18 | ||||
| chr2:17753725-17754162 | Common:3; Rare:141; Clinvar (benign):1 | ||||
| chr2:20051577-20051869 | Common:1; Rare:74 | ||||
| chr2:23927195-23927285 | Common:1; Rare:32 |