| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108482136-108482352 | Rare:46 | ||||
| chr2:108534203-108534477 | Common:7; Rare:113 | ||||
| chr2:108621129-108621280 | Rare:22 | ||||
| chr2:108719372-108719586 | Common:3; Rare:90; Clinvar (benign):2 | ||||
| chr2:109613823-109614038 | Common:2; Rare:74 | ||||
| chr2:110115633-110116001 | Common:4; Rare:99 | ||||
| chr2:111119313-111119388 | Common:1; Rare:20 | ||||
| chr2:111121141-111121165 | Rare:4 | ||||
| chr2:111122443-111122744 | Common:3; Rare:125 | ||||
| chr2:111884121-111884240 | Rare:36 | ||||
| chr2:111898300-111898660 | Common:2; Rare:79 | ||||
| chr2:112055461-112055601 | Common:2; Rare:38 | ||||
| chr2:112255004-112255152 | Common:1; Rare:65 | ||||
| chr2:112275392-112275657 | Common:1; Rare:91 | ||||
| chr2:112584358-112584639 | Common:1; Rare:75 |