Variant report

Variant	rs9766502
Chromosome Location	chr6:145984547-145984548
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145950800-145990600	Weak transcription	Primary B cells from cord blood	blood
2	chr6:145951000-146003000	Weak transcription	Thymus	Thymus
3	chr6:145951400-146003000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:145973600-145990600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:145974200-146002800	Weak transcription	Liver	Liver
6	chr6:145974800-146003600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr6:145980600-146010800	Weak transcription	Right Ventricle	heart
8	chr6:145982800-145989800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:145982800-146003000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr6:145984400-145984600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
11	chr6:145984400-145989400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:145984400-146003000	Weak transcription	Primary hematopoietic stem cells	blood

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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