Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:55544007-55544272 | Common:2; Rare:83 | ||||
chr2:55616557-55616616 | Common:1; Rare:15 | ||||
chr2:55618847-55618915 | Rare:23 | ||||
chr2:55693749-55694015 | Common:1; Rare:95; Clinvar (benign):2 | ||||
chr2:58046629-58046897 | Common:2; Rare:80 | ||||
chr2:58241303-58241401 | Rare:62; Clinvar:5; Clinvar (benign):1 | ||||
chr2:58241408-58241476 | Common:1; Rare:25 | ||||
chr2:60756113-60756416 | Rare:101 | ||||
chr2:60881268-60881690 | Common:2; Rare:147 | ||||
chr2:61017131-61017362 | Common:4; Rare:61 | ||||
chr2:61017419-61017756 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
chr2:61144907-61145192 | Common:3; Rare:92 | ||||
chr2:61177092-61177536 | Common:6; Rare:170 | ||||
chr2:61178025-61178320 | Common:2; Rare:89 | ||||
chr2:61185608-61185861 | Rare:87 |