| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112541828-112541965 | Common:2; Rare:35 | ||||
| chr2:112542047-112542535 | Common:2; Rare:159 | ||||
| chr2:112542584-112542723 | Common:1; Rare:46 | ||||
| chr2:112583477-112583749 | Rare:41 | ||||
| chr2:112584121-112584208 | Rare:14 | ||||
| chr2:112584251-112584974 | Common:2; Rare:193 | ||||
| chr2:112645237-112646078 | Common:4; Rare:240 | ||||
| chr2:112646229-112646449 | Common:2; Rare:75 | ||||
| chr2:112726007-112726261 | Rare:57 | ||||
| chr2:112763981-112764282 | Common:3; Rare:93 | ||||
| chr2:112764588-112764992 | Common:5; Rare:139; Clinvar (pathogenic):1 | ||||
| chr2:113157191-113157538 | Common:3; Rare:91 | ||||
| chr2:113157626-113157676 | Rare:11 | ||||
| chr2:113157726-113157783 | Rare:11 | ||||
| chr2:113198654-113198763 | Rare:26 |