Variant report

Variant	rs534200730
Chromosome Location	chr1:84236183-84236184
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33557	chr1:84236172-84236848	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84234600-84236200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr1:84234600-84236200	Enhancers	Primary B cells from peripheral blood	blood
3	chr1:84234600-84236400	Enhancers	Primary B cells from cord blood	blood
4	chr1:84234800-84236200	Enhancers	Fetal Brain Male	brain
5	chr1:84234800-84236200	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr1:84235000-84236400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:84235600-84236200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr1:84235800-84236200	Enhancers	Brain Substantia Nigra	brain
9	chr1:84236000-84237200	Enhancers	Liver	Liver

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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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