| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:196926653-196926827 | Common:2; Rare:81 | ||||
| chr2:197310590-197311040 | Common:1; Rare:104 | ||||
| chr2:197434991-197435303 | Rare:96 | ||||
| chr2:197453267-197453590 | Rare:120 | ||||
| chr2:197453871-197454021 | Rare:43 | ||||
| chr2:197499816-197500134 | Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500216-197500417 | Common:1; Rare:84 | ||||
| chr2:197515736-197516135 | Common:2; Rare:134 | ||||
| chr2:197675555-197676301 | Common:16; Rare:284 | ||||
| chr2:197705133-197705435 | Common:3; Rare:136; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197804251-197804801 | Common:6; Rare:250 | ||||
| chr2:199850860-199851646 | Common:4; Rare:318 | ||||
| chr2:199911001-199911387 | Common:2; Rare:114 | ||||
| chr2:199954995-199955395 | Common:4; Rare:122 | ||||
| chr2:199955439-199955589 | Rare:57 |