Variant report

Variant	rs11722282
Chromosome Location	chr4:91246336-91246337
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10015182	0.89[CEU][hapmap];0.94[EUR][1000 genomes]
rs1023905	0.90[CEU][hapmap];0.96[EUR][1000 genomes]
rs10516868	0.87[CEU][hapmap];0.94[EUR][1000 genomes]
rs11097246	0.94[EUR][1000 genomes]
rs11097247	0.81[CHB][hapmap]
rs11723677	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11943083	0.94[EUR][1000 genomes]
rs12108481	0.94[EUR][1000 genomes]
rs12108488	0.94[EUR][1000 genomes]
rs12639691	0.89[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12644644	0.96[EUR][1000 genomes]
rs12647511	0.96[EUR][1000 genomes]
rs13112637	0.94[EUR][1000 genomes]
rs13117351	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1461739	1.00[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1551794	0.84[CEU][hapmap];0.89[EUR][1000 genomes]
rs17016698	0.84[CEU][hapmap]
rs17016807	0.94[EUR][1000 genomes]
rs2054350	0.89[CEU][hapmap]
rs2085915	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs2085916	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs2126283	0.84[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34389744	0.91[EUR][1000 genomes]
rs34407211	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3775484	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6835475	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6842950	1.00[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs733660	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs752367	0.93[EUR][1000 genomes]
rs7654964	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7668943	0.94[EUR][1000 genomes]
rs7688401	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9993515	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470053	chr4:90879613-91439573	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv931074	chr4:90970476-91753697	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1007826	chr4:91049593-91438961	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv537177	chr4:91049593-91438961	Bivalent/Poised TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv999065	chr4:91049593-91520073	Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv879541	chr4:91156104-91253355	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv879542	chr4:91185206-91287204	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91228600-91249600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:91231800-91249600	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr4:91237800-91248200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr4:91238000-91249600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:91239200-91247800	Weak transcription	Fetal Kidney	kidney
6	chr4:91239400-91249600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:91239600-91249600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:91242800-91249800	Weak transcription	Left Ventricle	heart
9	chr4:91244600-91249400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:91244600-91249600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr4:91244600-91249600	Weak transcription	Gastric	stomach
12	chr4:91244600-91270200	Weak transcription	Pancreas	Pancrea
13	chr4:91244800-91249000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr4:91244800-91249800	Weak transcription	Fetal Stomach	stomach

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