Variant report

Variant	rs11119664
Chromosome Location	chr1:211199313-211199314
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10494931	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10494932	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11119658	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11119662	0.82[AFR][1000 genomes]
rs11578692	0.90[ASN][1000 genomes]
rs11579078	0.90[ASN][1000 genomes]
rs11582507	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11583101	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11588573	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12074568	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12121565	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12722738	0.96[ASN][1000 genomes]
rs12750762	0.90[ASN][1000 genomes]
rs12751504	0.86[ASN][1000 genomes]
rs12752336	0.86[ASN][1000 genomes]
rs12756697	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12760791	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1393028	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1501558	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1501560	0.82[CHB][hapmap];1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs1538287	0.84[JPT][hapmap]
rs1572646	0.84[JPT][hapmap]
rs17017226	0.84[JPT][hapmap]
rs17188741	0.82[ASN][1000 genomes]
rs17188748	0.80[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs17188797	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1933524	0.84[JPT][hapmap]
rs2134108	0.81[ASN][1000 genomes]
rs2221250	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs3111224	0.85[JPT][hapmap]
rs3120778	0.84[JPT][hapmap]
rs3125850	0.84[JPT][hapmap]
rs33985151	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs34773128	0.81[ASN][1000 genomes]
rs34827659	0.82[ASN][1000 genomes]
rs35019263	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs3828021	0.84[JPT][hapmap]
rs4262610	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4638187	0.90[ASN][1000 genomes]
rs56260926	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59374111	0.98[ASN][1000 genomes]
rs61850226	0.94[ASN][1000 genomes]
rs6540658	0.84[JPT][hapmap]
rs6669457	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs6669706	0.84[JPT][hapmap]
rs6683856	0.80[ASN][1000 genomes]
rs6697578	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6702598	0.90[ASN][1000 genomes]
rs7414286	0.90[ASN][1000 genomes]
rs7519090	0.94[ASN][1000 genomes]
rs867849	0.85[JPT][hapmap]
rs868963	0.82[CHB][hapmap];0.93[JPT][hapmap]
rs946142	0.85[JPT][hapmap]
rs9662051	0.82[ASN][1000 genomes]

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	nsv4410	chr1:211193724-211210571	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211182800-211228600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:211192600-211199800	Weak transcription	Brain Substantia Nigra	brain
3	chr1:211192600-211209000	Weak transcription	HSMMtube	muscle
4	chr1:211194400-211209200	Weak transcription	HSMM	muscle
5	chr1:211198600-211199400	Enhancers	Brain Hippocampus Middle	brain
6	chr1:211198800-211209600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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