Variant report

Variant	rs4951725
Chromosome Location	chr1:211334215-211334216
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12568832	0.85[ASN][1000 genomes]
rs12749443	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12758791	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17017239	0.95[ASN][1000 genomes]
rs2185069	0.95[ASN][1000 genomes]
rs35505648	0.94[ASN][1000 genomes]
rs35835736	0.85[ASN][1000 genomes]
rs3811394	0.87[ASN][1000 genomes]
rs4951720	0.93[ASN][1000 genomes]
rs4951727	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55824853	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56317037	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56367975	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs867847	0.95[ASN][1000 genomes]
rs867848	0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211334200-211340400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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