Variant report

Variant	rs11029577
Chromosome Location	chr11:26499535-26499536
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10767536	0.82[EUR][1000 genomes]
rs10767537	0.82[EUR][1000 genomes]
rs10767540	0.81[EUR][1000 genomes]
rs10767541	0.81[EUR][1000 genomes]
rs10767545	0.81[EUR][1000 genomes]
rs10834983	0.81[EUR][1000 genomes]
rs10834984	0.81[EUR][1000 genomes]
rs10834985	0.81[EUR][1000 genomes]
rs10834986	0.81[GIH][hapmap];0.91[TSI][hapmap];0.81[EUR][1000 genomes]
rs10834987	0.81[EUR][1000 genomes]
rs10834988	0.81[EUR][1000 genomes]
rs10834989	0.81[EUR][1000 genomes]
rs10834990	0.81[EUR][1000 genomes]
rs10834991	0.80[EUR][1000 genomes]
rs10834992	0.81[EUR][1000 genomes]
rs10834993	0.81[EUR][1000 genomes]
rs10834994	0.81[EUR][1000 genomes]
rs10834996	0.81[EUR][1000 genomes]
rs10834997	0.81[EUR][1000 genomes]
rs11029571	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11029574	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11029576	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11029588	0.81[EUR][1000 genomes]
rs1125621	0.81[GIH][hapmap];0.91[TSI][hapmap];0.81[EUR][1000 genomes]
rs1125622	0.81[EUR][1000 genomes]
rs1125623	0.81[EUR][1000 genomes]
rs1125624	0.81[EUR][1000 genomes]
rs12290380	0.82[EUR][1000 genomes]
rs1355131	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1355132	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1493739	0.82[MEX][hapmap]
rs1602938	0.81[EUR][1000 genomes]
rs1602939	0.81[EUR][1000 genomes]
rs2087974	0.86[CEU][hapmap];0.98[GIH][hapmap];0.86[MEX][hapmap];0.90[TSI][hapmap];0.91[EUR][1000 genomes]
rs2131697	0.90[YRI][hapmap];0.87[AFR][1000 genomes]
rs2860040	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs294015	0.82[TSI][hapmap]
rs294018	0.82[TSI][hapmap]
rs294028	0.82[TSI][hapmap]
rs4418757	0.82[EUR][1000 genomes]
rs4923360	0.83[EUR][1000 genomes]
rs7119659	1.00[CEU][hapmap];0.83[JPT][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7128699	0.82[EUR][1000 genomes]
rs721258	0.86[CEU][hapmap];0.93[EUR][1000 genomes]
rs72889134	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7929215	0.81[EUR][1000 genomes]
rs7929544	0.81[EUR][1000 genomes]
rs7935953	0.81[EUR][1000 genomes]
rs7942067	0.89[GIH][hapmap]
rs7944026	0.81[EUR][1000 genomes]
rs7944034	0.81[EUR][1000 genomes]
rs903155	0.81[GIH][hapmap]

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	nsv1051211	chr11:26473131-26604553	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv467778	chr11:26485520-26603926	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv553899	chr11:26485520-26603926	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv521916	chr11:26485520-26605331	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26472000-26503600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr11:26498800-26499600	Enhancers	Stomach Mucosa	stomach

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