Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:197590957-197590966 | Rare:6 | ||||
chr2:197706693-197706747 | Rare:20; Clinvar (benign):1 | ||||
chr2:201970691-201970950 | Rare:44 | ||||
chr2:202035520-202035934 | Rare:128 | ||||
chr2:202036013-202036293 | Rare:86 | ||||
chr2:202036298-202036377 | Rare:21 | ||||
chr2:202036785-202036985 | Rare:35 | ||||
chr2:202037369-202037702 | Common:2; Rare:42 | ||||
chr2:202376074-202376186 | Rare:48 | ||||
chr2:206083798-206083987 | Common:2; Rare:26 | ||||
chr2:206809933-206810146 | Rare:57 | ||||
chr2:206812199-206812438 | Common:1; Rare:50 | ||||
chr2:209299449-209299821 | Common:1; Rare:100 | ||||
chr2:209301430-209301595 | Common:3; Rare:48 | ||||
chr2:209301645-209301667 | Rare:5 |