Variant report

Variant	rs7326209
Chromosome Location	chr13:50419482-50419483
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1407439	0.86[CEU][hapmap];0.89[CHB][hapmap]
rs3742096	0.91[CEU][hapmap];0.89[CHB][hapmap]
rs7324563	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7328465	0.80[EUR][1000 genomes]
rs7332209	0.89[CHB][hapmap]
rs748678	0.86[CEU][hapmap]
rs7982919	0.82[CEU][hapmap];0.90[CHB][hapmap]
rs7983049	0.81[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs7996689	0.86[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes]
rs9316478	0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9535346	0.89[CHB][hapmap]
rs9535351	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs9535360	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9535361	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9535362	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9535366	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50411400-50422000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr13:50413000-50421600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr13:50415000-50420600	Weak transcription	K562	blood
4	chr13:50415400-50421600	Weak transcription	HepG2	liver
5	chr13:50415400-50421800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr13:50415600-50421800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr13:50417600-50421800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr13:50418800-50421800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr13:50418800-50421800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr13:50418800-50421800	Weak transcription	NHDF-Ad	bronchial

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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