Variant report

Variant	rs11768629
Chromosome Location	chr7:104102770-104102771
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10232719	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10239251	1.00[CEU][hapmap];0.88[CHB][hapmap];0.90[JPT][hapmap];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10248554	0.88[EUR][1000 genomes]
rs10248577	0.86[EUR][1000 genomes]
rs10248586	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10248725	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10248853	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10252016	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10253179	1.00[CEU][hapmap];0.88[CHB][hapmap];0.90[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10258646	0.88[EUR][1000 genomes]
rs10263143	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10267229	0.91[EUR][1000 genomes]
rs10267467	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10268222	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs10278196	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10279103	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11763095	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11768543	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12112342	1.00[CEU][hapmap];0.86[YRI][hapmap]
rs12705211	0.93[CEU][hapmap];0.88[CHB][hapmap];0.81[JPT][hapmap];0.88[ASN][1000 genomes]
rs12705212	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12705213	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12705217	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13223335	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13224554	1.00[CEU][hapmap];0.96[YRI][hapmap]
rs1858780	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs28504445	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28590508	0.92[ASN][1000 genomes]
rs6977154	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7796342	1.00[CEU][hapmap]
rs7806966	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7807089	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7811730	1.00[CEU][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888925	chr7:104047599-104170560	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	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