Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:16185943-16186053 | Rare:20 | ||||
chr2:16186066-16186252 | Common:1; Rare:43 | ||||
chr2:16194680-16194863 | Rare:40 | ||||
chr2:16197410-16197551 | Rare:16 | ||||
chr2:16197592-16197713 | Common:2; Rare:26 | ||||
chr2:16197724-16198074 | Common:3; Rare:71 | ||||
chr2:16198308-16198750 | Common:1; Rare:101 | ||||
chr2:21282218-21282370 | Rare:33 | ||||
chr2:22879039-22879332 | Common:5; Rare:57 | ||||
chr2:23351579-23351780 | Common:1; Rare:50 | ||||
chr2:25315112-25315199 | Rare:17 | ||||
chr2:26652606-26652884 | Common:2; Rare:47 | ||||
chr2:26749940-26750164 | Common:1; Rare:44 | ||||
chr2:27752564-27752917 | Rare:51 | ||||
chr2:28664258-28664476 | Common:3; Rare:32 |