| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:172102900-172103045 | Common:1; Rare:35 | ||||
| chr2:172427429-172427791 | Common:6; Rare:105; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:172555893-172556234 | Common:2; Rare:123 | ||||
| chr2:172859905-172860176 | Rare:45 | ||||
| chr2:173354584-173354966 | Common:1; Rare:116 | ||||
| chr2:173963782-173964351 | Common:1; Rare:244 | ||||
| chr2:173965241-173965541 | Common:2; Rare:107 | ||||
| chr2:174248454-174248828 | Common:2; Rare:122 | ||||
| chr2:174395618-174395812 | Common:2; Rare:62 | ||||
| chr2:174487027-174487439 | Common:2; Rare:109 | ||||
| chr2:174682861-174683012 | Common:1; Rare:61 | ||||
| chr2:175005156-175005357 | Common:2; Rare:70; Clinvar:2 | ||||
| chr2:175167666-175167845 | Rare:61 | ||||
| chr2:175167875-175167919 | Rare:7 | ||||
| chr2:175168104-175168593 | Common:2; Rare:134 |