Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:18955329-18955425 | Rare:14 | ||||
chr1:18955659-18956026 | Rare:82 | ||||
chr1:18956618-18956972 | Common:3; Rare:97 | ||||
chr1:19077421-19077472 | Rare:6 | ||||
chr1:19210244-19210422 | Rare:69 | ||||
chr1:19251479-19251842 | Common:6; Rare:126 | ||||
chr1:19311982-19312350 | Common:8; Rare:168 | ||||
chr1:19596897-19597087 | Common:2; Rare:96 | ||||
chr1:20508079-20508205 | Common:2; Rare:46 | ||||
chr1:20637622-20637883 | Common:4; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr1:20786631-20786773 | Rare:49 | ||||
chr1:21345463-21345640 | Common:2; Rare:70 | ||||
chr1:21782945-21783249 | Common:2; Rare:101 | ||||
chr1:21847782-21847959 | Common:2; Rare:65 | ||||
chr1:22053501-22053566 | Common:1; Rare:18 |