| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171999837-171999988 | Common:1; Rare:61 | ||||
| chr2:172427389-172427725 | Common:9; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172555876-172556300 | Common:3; Rare:147 | ||||
| chr2:172556427-172556695 | Common:1; Rare:74 | ||||
| chr2:173075225-173075496 | Common:2; Rare:44 | ||||
| chr2:173075923-173075983 | Common:1; Rare:22 | ||||
| chr2:173159756-173160007 | Common:1; Rare:35 | ||||
| chr2:173354618-173354930 | Common:1; Rare:99 | ||||
| chr2:173964477-173964628 | Rare:73 | ||||
| chr2:173965164-173965519 | Common:1; Rare:127 | ||||
| chr2:173965822-173965913 | Rare:31 | ||||
| chr2:174395616-174395964 | Common:2; Rare:105 | ||||
| chr2:174846940-174847298 | Common:1; Rare:77 | ||||
| chr2:174847529-174847724 | Rare:40 | ||||
| chr2:175129893-175129993 | Common:1; Rare:18 |