| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191014017-191014478 | Common:3; Rare:144; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:191245098-191245619 | Common:4; Rare:159 | ||||
| chr2:191377759-191378035 | Common:2; Rare:47 | ||||
| chr2:191401691-191401837 | Common:1; Rare:21 | ||||
| chr2:191677759-191678272 | Common:4; Rare:135 | ||||
| chr2:191678499-191678663 | Rare:56 | ||||
| chr2:192194881-192195034 | Rare:32 | ||||
| chr2:195656571-195656784 | Rare:39 | ||||
| chr2:195656876-195656960 | Rare:26 | ||||
| chr2:195657052-195657351 | Common:1; Rare:91 | ||||
| chr2:196799554-196799738 | Common:1; Rare:66 | ||||
| chr2:196926619-196926814 | Common:2; Rare:87 | ||||
| chr2:197310620-197310806 | Common:1; Rare:40 | ||||
| chr2:197402549-197403030 | Rare:69; Clinvar (pathogenic):4 | ||||
| chr2:197434973-197435222 | Rare:83 |