| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96740048-96740308 | Common:5; Rare:58 | ||||
| chr2:96816039-96816273 | Common:3; Rare:89 | ||||
| chr2:96840893-96841169 | Common:3; Rare:69 | ||||
| chr2:97113069-97113245 | Rare:41 | ||||
| chr2:97113457-97113691 | Rare:54 | ||||
| chr2:97663902-97664261 | Common:1; Rare:110 | ||||
| chr2:97995591-97995923 | Common:3; Rare:102 | ||||
| chr2:97995926-97996196 | Rare:97 | ||||
| chr2:98608311-98608636 | Common:1; Rare:134; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98731047-98731308 | Common:3; Rare:88 | ||||
| chr2:98869215-98869518 | Common:3; Rare:64 | ||||
| chr2:99141128-99141489 | Common:1; Rare:134 | ||||
| chr2:99141639-99141794 | Rare:37 | ||||
| chr2:99154877-99155041 | Common:1; Rare:69; Clinvar (benign):2 | ||||
| chr2:99180853-99181220 | Common:2; Rare:121 |