Variant report

Variant	rs17104611
Chromosome Location	chr11:105700180-105700181
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11226826	0.91[CHD][hapmap];0.86[JPT][hapmap]
rs11226850	1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap]
rs17104532	1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap]
rs17104549	1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.85[AMR][1000 genomes]
rs17104577	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17104583	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs17104598	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17104609	1.00[ASW][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2121062	0.91[CHD][hapmap];0.86[JPT][hapmap]
rs41445847	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs561015	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs597395	1.00[CHB][hapmap];0.90[CHD][hapmap];0.86[JPT][hapmap]
rs626633	1.00[CHB][hapmap];0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs635980	0.91[CHD][hapmap];0.86[JPT][hapmap]
rs641435	1.00[CHB][hapmap];0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs643063	1.00[CHB][hapmap];0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs667713	0.86[JPT][hapmap]
rs7108004	1.00[CHB][hapmap]
rs7119216	1.00[CHB][hapmap];0.86[JPT][hapmap];0.85[AMR][1000 genomes]
rs7124769	1.00[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs72987139	0.80[ASN][1000 genomes]
rs72987142	0.80[ASN][1000 genomes]
rs73554208	0.90[ASN][1000 genomes]
rs7938516	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7947803	0.86[JPT][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	nsv898357	chr11:105614894-105709856	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv832257	chr11:105662753-105817576	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	esv1825856	chr11:105672706-105775768	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1825993	chr11:105698982-105762601	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105691400-105702000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:105699800-105700600	Enhancers	Primary B cells from peripheral blood	blood
3	chr11:105700000-105700400	Enhancers	GM12878-XiMat	blood
4	chr11:105700000-105700400	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr11:105700000-105700600	Enhancers	Primary monocytes fromperipheralblood	blood

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