Variant report

Variant	rs1605292
Chromosome Location	chr11:93647354-93647355
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1032934	1.00[CEU][hapmap];0.86[AFR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1032935	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10501811	0.91[ASN][1000 genomes]
rs11020587	1.00[CEU][hapmap];0.96[AFR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1113700	0.96[ASN][1000 genomes]
rs12270580	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1401184	1.00[CEU][hapmap]
rs1605293	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2019595	0.93[ASN][1000 genomes]
rs2203793	1.00[CEU][hapmap]
rs2460047	0.96[ASN][1000 genomes]
rs2460065	1.00[CEU][hapmap]
rs2462733	1.00[CEU][hapmap]
rs2462735	1.00[CEU][hapmap]
rs2462758	1.00[CEU][hapmap]
rs4590831	0.90[AFR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57214110	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57367718	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59013509	0.96[ASN][1000 genomes]
rs60539088	0.94[ASN][1000 genomes]
rs61463513	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6483278	0.89[EUR][1000 genomes]
rs66650995	0.94[ASN][1000 genomes]
rs67689846	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67926172	0.94[ASN][1000 genomes]
rs68019383	0.94[ASN][1000 genomes]
rs7102891	0.96[AFR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72962832	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72962854	0.94[ASN][1000 genomes]
rs7932631	0.95[AFR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs908754	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs978950	0.96[AFR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs978952	0.91[AFR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv508650	chr11:93609010-93713576	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	esv1796911	chr11:93642877-93688134	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93641600-93652800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:93642000-93655200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:93642200-93649800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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