| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171922273-171922506 | Rare:163 | ||||
| chr2:171999785-172000014 | Common:3; Rare:168 | ||||
| chr2:172084617-172084831 | Rare:90 | ||||
| chr2:172102868-172103084 | Common:3; Rare:96 | ||||
| chr2:172427477-172427749 | Common:4; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172555897-172556159 | Common:4; Rare:197 | ||||
| chr2:172556390-172556960 | Common:1; Rare:147 | ||||
| chr2:173075777-173075979 | Common:1; Rare:103 | ||||
| chr2:173354562-173354946 | Common:2; Rare:210 | ||||
| chr2:173963809-173963997 | Common:2; Rare:177 | ||||
| chr2:173963998-173964412 | Rare:328 | ||||
| chr2:173964546-173964884 | Common:1; Rare:157 | ||||
| chr2:173965251-173965547 | Common:3; Rare:197 | ||||
| chr2:173965806-173965973 | Rare:121 | ||||
| chr2:174248447-174248763 | Common:2; Rare:189 |