| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:196926600-196927184 | Common:4; Rare:188 | ||||
| chr2:197310404-197310659 | Common:3; Rare:75 | ||||
| chr2:197310725-197310868 | Rare:30 | ||||
| chr2:197434546-197434636 | Rare:13 | ||||
| chr2:197434738-197435399 | Common:1; Rare:179 | ||||
| chr2:197453069-197453633 | Rare:195 | ||||
| chr2:197453737-197454047 | Common:1; Rare:88 | ||||
| chr2:197499303-197499441 | Rare:53 | ||||
| chr2:197499680-197500472 | Common:2; Rare:289; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:197515698-197516180 | Common:2; Rare:163 | ||||
| chr2:197516574-197516611 | Rare:10 | ||||
| chr2:197704988-197705526 | Common:3; Rare:226; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:197804418-197804605 | Rare:42 | ||||
| chr2:199850808-199850994 | Rare:35 | ||||
| chr2:199851039-199851322 | Common:1; Rare:88 |