| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:196260097-196260149 | Rare:12 | ||||
| chr2:197488486-197488760 | Common:3; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:201121344-201121378 | Rare:5 | ||||
| chr2:201123965-201124082 | Rare:17 | ||||
| chr2:201124141-201124480 | Common:2; Rare:53 | ||||
| chr2:201152637-201152721 | Common:2; Rare:18 | ||||
| chr2:202375526-202375875 | Common:1; Rare:74 | ||||
| chr2:203447993-203448139 | Rare:23 | ||||
| chr2:203477100-203477375 | Rare:51 | ||||
| chr2:206085186-206085252 | Rare:18 | ||||
| chr2:207742976-207743107 | Rare:24 | ||||
| chr2:207761239-207761393 | Rare:34 | ||||
| chr2:210172053-210172091 | Rare:7 | ||||
| chr2:210427590-210427813 | Common:1; Rare:41 | ||||
| chr2:212537585-212537884 | Common:2; Rare:66 |