Variant report

Variant	rs11229172
Chromosome Location	chr11:57710046-57710047
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10792118	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10896644	0.83[YRI][hapmap]
rs11229170	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11229171	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11229173	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11229183	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11570176	0.83[YRI][hapmap]
rs11570181	0.83[YRI][hapmap]
rs12366063	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12420220	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1510418	0.81[EUR][1000 genomes]
rs17455422	0.83[YRI][hapmap]
rs1848879	0.86[EUR][1000 genomes]
rs34419144	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35241049	0.81[EUR][1000 genomes]
rs35994197	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4245215	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4272798	0.80[AMR][1000 genomes]
rs588713	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs588808	0.80[ASN][1000 genomes]
rs591322	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs593239	0.85[EUR][1000 genomes]
rs600488	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs602861	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs606731	0.88[EUR][1000 genomes]
rs615133	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs616911	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61905278	0.80[ASN][1000 genomes]
rs626043	0.84[EUR][1000 genomes]
rs633129	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs636388	0.85[EUR][1000 genomes]
rs652191	0.85[YRI][hapmap]
rs653889	0.83[YRI][hapmap]
rs6591443	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs662638	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs681397	0.90[EUR][1000 genomes]
rs7103977	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7106195	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7119973	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7120868	0.83[YRI][hapmap]
rs7926999	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7943793	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]

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	nsv1044030	chr11:57073395-58035564	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	nsv541047	chr11:57073395-58035564	Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
3	nsv1054205	chr11:57544264-58358509	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
4	nsv897589	chr11:57623815-58052357	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11229172	YPEL4	cis	lung	GTEx

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57707400-57710600	Enhancers	NHEK	skin
2	chr11:57707600-57710600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr11:57707600-57710600	Enhancers	HepG2	liver
4	chr11:57709400-57710200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr11:57709400-57710600	Enhancers	Esophagus	oesophagus
6	chr11:57709600-57710400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:57709800-57713400	Weak transcription	Lung	lung

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