Variant report

Variant	rs9568339
Chromosome Location	chr13:50436185-50436186
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11618972	0.98[ASN][1000 genomes]
rs2407706	0.84[ASN][1000 genomes]
rs4942887	0.96[ASN][1000 genomes]
rs55684391	0.98[ASN][1000 genomes]
rs7139851	0.96[ASN][1000 genomes]
rs7983607	0.92[ASN][1000 genomes]
rs9526613	0.96[ASN][1000 genomes]
rs9526615	0.95[ASN][1000 genomes]
rs9535384	0.96[ASN][1000 genomes]
rs9535385	0.96[ASN][1000 genomes]
rs9535387	0.93[ASN][1000 genomes]
rs9568340	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9568341	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9568342	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50422200-50436600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr13:50434000-50438200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:50434200-50442000	Weak transcription	Pancreas	Pancrea

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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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