Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:46340945-46341191 | Common:1; Rare:61 | ||||
chr1:46394135-46394366 | Rare:64 | ||||
chr1:46604196-46604489 | Common:1; Rare:82 | ||||
chr1:46616617-46616662 | Rare:7 | ||||
chr1:46616791-46616944 | Common:2; Rare:38 | ||||
chr1:46667935-46668098 | Rare:47 | ||||
chr1:46668279-46668675 | Common:3; Rare:119 | ||||
chr1:46719080-46719354 | Rare:101 | ||||
chr1:46719387-46719411 | Common:1; Rare:4 | ||||
chr1:47231819-47231965 | Common:1; Rare:28 | ||||
chr1:47232406-47232435 | Rare:7 | ||||
chr1:47313514-47313624 | Common:1; Rare:15 | ||||
chr1:47313975-47314564 | Common:5; Rare:132; Clinvar:3; Clinvar (benign):1 | ||||
chr1:47333489-47333968 | Common:4; Rare:138 | ||||
chr1:47334002-47334047 | Rare:19 |