| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171894200-171894396 | Rare:164; Clinvar:3 | ||||
| chr2:171922256-171922526 | Rare:183 | ||||
| chr2:171999817-172000051 | Common:2; Rare:150 | ||||
| chr2:172084530-172084760 | Common:1; Rare:55 | ||||
| chr2:172102896-172103033 | Common:1; Rare:34 | ||||
| chr2:172427360-172427715 | Common:13; Rare:160; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:172555360-172555720 | Common:4; Rare:142 | ||||
| chr2:172555844-172556159 | Common:6; Rare:250 | ||||
| chr2:172556420-172557070 | Common:3; Rare:257 | ||||
| chr2:172859690-172860200 | Common:1; Rare:128 | ||||
| chr2:173075738-173075994 | Common:1; Rare:120 | ||||
| chr2:173159670-173160050 | Common:1; Rare:56 | ||||
| chr2:173354534-173354935 | Common:2; Rare:229 | ||||
| chr2:173963799-173964650 | Common:2; Rare:620 | ||||
| chr2:173965258-173965518 | Common:2; Rare:180 |