| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:58047224-58047274 | Rare:16 | ||||
| chr2:58241316-58241392 | Rare:48; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:60553627-60553848 | Rare:41 | ||||
| chr2:60756148-60756296 | Rare:53 | ||||
| chr2:60881315-60881664 | Common:2; Rare:134 | ||||
| chr2:61017191-61017770 | Common:4; Rare:173; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61144916-61145175 | Common:3; Rare:84 | ||||
| chr2:61177182-61177458 | Common:5; Rare:114 | ||||
| chr2:61471246-61471386 | Common:2; Rare:51 | ||||
| chr2:61888493-61888720 | Common:1; Rare:96 | ||||
| chr2:63588226-63588557 | Common:1; Rare:102; Clinvar:6 | ||||
| chr2:63588610-63589027 | Common:1; Rare:127; Clinvar (benign):1 | ||||
| chr2:63840807-63841171 | Common:2; Rare:104 | ||||
| chr2:63841614-63841897 | Common:2; Rare:95 | ||||
| chr2:64019414-64019491 | Rare:30 |