| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55617520-55618861 | Common:13; Rare:502 | ||||
| chr2:55618793-55619027 | Common:1; Rare:94 | ||||
| chr2:55693713-55693993 | Common:1; Rare:211; Clinvar (benign):6 | ||||
| chr2:55923250-55923650 | Common:2; Rare:85 | ||||
| chr2:55923701-55923930 | Common:5; Rare:124; Clinvar:1; Clinvar (benign):12 | ||||
| chr2:56183637-56184108 | Common:25; Rare:239 | ||||
| chr2:56184239-56184640 | Common:2; Rare:124 | ||||
| chr2:58046401-58047691 | Common:10; Rare:700 | ||||
| chr2:58240941-58241050 | Rare:38 | ||||
| chr2:58241263-58241501 | Common:2; Rare:260; Clinvar:13; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:60755983-60756382 | Common:1; Rare:212 | ||||
| chr2:60756700-60757150 | Common:3; Rare:118 | ||||
| chr2:60881316-60881778 | Common:8; Rare:380 | ||||
| chr2:61016458-61016858 | Common:1; Rare:114 | ||||
| chr2:61016900-61017261 | Common:9; Rare:200 |