| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96208252-96208502 | Rare:118 | ||||
| chr2:96208776-96208955 | Common:4; Rare:74 | ||||
| chr2:96265940-96266499 | Common:2; Rare:157; Clinvar:2 | ||||
| chr2:96305443-96305638 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96335707-96335828 | Common:1; Rare:41 | ||||
| chr2:96816039-96816272 | Common:3; Rare:89 | ||||
| chr2:96869381-96869590 | Common:2; Rare:51 | ||||
| chr2:96869896-96870171 | Common:2; Rare:59 | ||||
| chr2:97645887-97646187 | Common:3; Rare:90 | ||||
| chr2:97663993-97664272 | Rare:79 | ||||
| chr2:98608415-98608643 | Common:1; Rare:100; Clinvar (benign):1 | ||||
| chr2:99141139-99141494 | Common:1; Rare:129 | ||||
| chr2:99141523-99141588 | Common:1; Rare:35 | ||||
| chr2:99154886-99155121 | Common:3; Rare:94; Clinvar (benign):3 | ||||
| chr2:99180858-99181252 | Common:2; Rare:128 |