Variant report

Variant	rs6798617
Chromosome Location	chr3:34608785-34608786
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11129598	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13074645	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1520626	0.83[AFR][1000 genomes]
rs1520641	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1520644	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1851057	0.81[AMR][1000 genomes]
rs2167041	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2167042	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4678695	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7614078	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7629903	0.83[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs918085	0.81[AMR][1000 genomes]
rs9860621	0.93[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34607200-34609200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:34608000-34611400	Enhancers	Fetal Heart	heart
3	chr3:34608600-34609000	Enhancers	Fetal Brain Female	brain

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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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