Variant report

Variant	rs4773813
Chromosome Location	chr13:95410508-95410509
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1924075	0.93[ASN][1000 genomes]
rs1924076	0.93[ASN][1000 genomes]
rs4771893	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6492744	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7330451	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs882514	0.83[ASN][1000 genomes]
rs9301996	1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.83[ASN][1000 genomes]
rs9516470	0.93[ASN][1000 genomes]
rs9524607	0.83[ASN][1000 genomes]
rs9524609	0.83[ASN][1000 genomes]
rs9524610	0.83[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95409600-95412800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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

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