Variant report

Variant	rs6776111
Chromosome Location	chr3:68416163-68416164
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs17047606	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17047609	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs17047611	0.90[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs2221759	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs262186	0.94[CHB][hapmap];0.86[JPT][hapmap]
rs262190	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs262193	0.94[CHB][hapmap];0.81[JPT][hapmap]
rs262200	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs262202	0.95[CHB][hapmap];0.93[JPT][hapmap]
rs262204	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs262206	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs262226	0.89[CHB][hapmap];0.80[JPT][hapmap];0.88[ASN][1000 genomes]
rs262227	0.89[CHB][hapmap];0.80[JPT][hapmap];0.88[ASN][1000 genomes]
rs262234	0.89[CHB][hapmap]
rs262237	0.85[CHB][hapmap]
rs262238	0.84[CHB][hapmap]
rs262241	0.84[CHB][hapmap]
rs262242	0.85[CHB][hapmap]
rs262244	0.88[CHB][hapmap]
rs63108	0.84[CHB][hapmap]
rs6769848	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6774356	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[YRI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6792971	0.90[CEU][hapmap]
rs6805785	1.00[CEU][hapmap];0.90[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap]
rs7610318	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs7617495	1.00[CEU][hapmap];0.90[CHB][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7629299	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs7629408	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7639960	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs7642781	0.90[CHB][hapmap];0.87[JPT][hapmap]
rs952768	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs957895	1.00[CEU][hapmap];0.90[CHB][hapmap];0.94[YRI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752014	chr3:68091879-68416989	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv834721	chr3:68365963-68526394	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv590562	chr3:68393781-68422687	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
4	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

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

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links