Variant report

Variant	rs7629385
Chromosome Location	chr3:68418867-68418868
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13340202	1.00[JPT][hapmap]
rs17047523	1.00[JPT][hapmap]
rs17047525	1.00[JPT][hapmap]
rs17047573	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs17396472	1.00[JPT][hapmap]
rs1873596	1.00[JPT][hapmap]
rs1873597	1.00[JPT][hapmap]
rs6778918	1.00[CEU][hapmap]
rs6780812	1.00[CEU][hapmap]
rs6798891	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs73836901	1.00[EUR][1000 genomes]
rs7617495	0.84[YRI][hapmap];0.83[AFR][1000 genomes]
rs7618788	1.00[JPT][hapmap]
rs7639960	0.92[YRI][hapmap]
rs7640148	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834721	chr3:68365963-68526394	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv590562	chr3:68393781-68422687	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
3	nsv590563	chr3:68402933-68422687	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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