| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108719404-108719625 | Common:2; Rare:90; Clinvar (benign):2 | ||||
| chr2:109613835-109614008 | Common:2; Rare:64 | ||||
| chr2:110204941-110205072 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:111122436-111122764 | Common:3; Rare:132 | ||||
| chr2:111884170-111884240 | Rare:16 | ||||
| chr2:112055480-112055589 | Common:2; Rare:29 | ||||
| chr2:112275404-112275622 | Common:1; Rare:68 | ||||
| chr2:112542129-112542504 | Common:2; Rare:117 | ||||
| chr2:112584362-112584633 | Common:1; Rare:72 | ||||
| chr2:112584772-112584834 | Rare:17 | ||||
| chr2:112645709-112645947 | Common:1; Rare:88 | ||||
| chr2:113437592-113437861 | Common:2; Rare:96 | ||||
| chr2:113627041-113627303 | Common:3; Rare:78 | ||||
| chr2:113756507-113756742 | Common:2; Rare:71 | ||||
| chr2:113889753-113890165 | Common:8; Rare:132 |