Variant report

Variant	rs11031911
Chromosome Location	chr11:32659585-32659586
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:32659336..32661758-chr11:32663694..32666060,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10835948	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.86[ASN][1000 genomes]
rs10835957	1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[YRI][hapmap]
rs10835980	0.81[ASN][1000 genomes]
rs11031885	1.00[CHB][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes]
rs11031895	0.89[ASN][1000 genomes]
rs11031896	0.89[ASN][1000 genomes]
rs11031902	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11031953	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11031967	1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs11031968	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs11031974	0.84[ASN][1000 genomes]
rs11031993	0.81[ASN][1000 genomes]
rs11032011	0.81[ASN][1000 genomes]
rs11820154	0.81[ASN][1000 genomes]
rs12363452	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12363973	1.00[CHB][hapmap];0.85[JPT][hapmap];0.87[YRI][hapmap];0.81[ASN][1000 genomes]
rs12366254	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12574799	0.81[ASN][1000 genomes]
rs12787879	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.87[YRI][hapmap];0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12791629	0.81[ASN][1000 genomes]
rs12796379	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12801320	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap]
rs12802087	0.87[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs1352177	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1352178	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17251664	1.00[CHB][hapmap];0.85[JPT][hapmap];0.87[YRI][hapmap];0.81[ASN][1000 genomes]
rs17327768	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.81[ASN][1000 genomes]
rs17329869	1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[YRI][hapmap];0.81[ASN][1000 genomes]
rs201842	0.92[YRI][hapmap]
rs2087085	1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs33992831	0.89[ASN][1000 genomes]
rs34370631	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35733667	0.81[ASN][1000 genomes]
rs4267044	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs4756174	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58910879	0.81[ASN][1000 genomes]
rs61889448	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7108031	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.86[ASN][1000 genomes]
rs7113466	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs7115208	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7121691	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7129747	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7130509	0.82[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs7130754	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7933005	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs7934364	1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.86[ASN][1000 genomes]
rs7942369	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7949244	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap]
rs9667005	0.87[ASN][1000 genomes]
rs9734816	0.87[ASN][1000 genomes]
rs9736074	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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	esv3424973	chr11:32633425-32664062	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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