| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171687401-171687918 | Common:1; Rare:113 | ||||
| chr2:171922236-171922560 | Rare:118 | ||||
| chr2:171999833-171999964 | Common:1; Rare:57 | ||||
| chr2:172427523-172427725 | Common:3; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172487982-172488226 | Common:1; Rare:66; Clinvar:1 | ||||
| chr2:172491089-172491304 | Common:2; Rare:64; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:172555908-172556159 | Common:1; Rare:95 | ||||
| chr2:172556431-172556646 | Common:1; Rare:59 | ||||
| chr2:172735775-172735958 | Common:1; Rare:45 | ||||
| chr2:173075262-173075588 | Common:4; Rare:60 | ||||
| chr2:173075795-173075867 | Rare:18 | ||||
| chr2:173354497-173354958 | Common:1; Rare:139 | ||||
| chr2:173963761-173963992 | Common:1; Rare:105 | ||||
| chr2:173964008-173964363 | Rare:145 | ||||
| chr2:173965260-173965518 | Common:1; Rare:92 |