| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:196799558-196799824 | Common:4; Rare:144 | ||||
| chr2:196926580-196927220 | Common:6; Rare:283; Clinvar:1 | ||||
| chr2:197310726-197310841 | Rare:21 | ||||
| chr2:197434978-197435288 | Rare:193 | ||||
| chr2:197453214-197453554 | Rare:222 | ||||
| chr2:197499799-197500441 | Common:2; Rare:452; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:197515876-197516132 | Common:1; Rare:174 | ||||
| chr2:197705186-197705461 | Common:6; Rare:234; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:199457380-199457900 | Common:1; Rare:178 | ||||
| chr2:199457920-199458410 | Common:4; Rare:150 | ||||
| chr2:199459210-199459801 | Common:3; Rare:274 | ||||
| chr2:199851000-199851580 | Common:3; Rare:208 | ||||
| chr2:199910960-199911460 | Common:2; Rare:283 | ||||
| chr2:199911510-199911790 | Common:2; Rare:156 | ||||
| chr2:200306418-200306770 | Common:8; Rare:192 |