Variant report

Variant rs566118603
Chromosome Location chr2:180066987-180066988
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180032200-180067600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:180065600-180068200 Weak transcription Fetal Stomach stomach
3 chr2:180066400-180067000 Weak transcription Primary hematopoietic stem cells blood
4 chr2:180066800-180067600 ZNF genes & repeats Fetal Kidney kidney
5 chr2:180066800-180067800 ZNF genes & repeats HepG2 liver
6 chr2:180066800-180068400 ZNF genes & repeats Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:180066800-180068800 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell

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