Variant report

Variant	rs13202733
Chromosome Location	chr6:163802590-163802591
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:163801051..163802963-chr6:163805360..163807590,2	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11760168	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11962088	0.89[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs13202116	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13204052	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1336223	0.87[ASN][1000 genomes]
rs1336224	0.87[ASN][1000 genomes]
rs1336225	0.87[ASN][1000 genomes]
rs1414724	0.85[ASN][1000 genomes]
rs1591536	0.85[ASN][1000 genomes]
rs16894934	0.82[ASN][1000 genomes]
rs16895015	0.82[JPT][hapmap]
rs1737319	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs1737321	0.89[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs1737322	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs1737324	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1737328	0.89[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs1764009	0.84[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs1764010	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs1764011	0.90[CHB][hapmap];1.00[JPT][hapmap]
rs1764015	0.85[ASN][1000 genomes]
rs1764019	0.85[ASN][1000 genomes]
rs1764020	0.97[ASN][1000 genomes]
rs2064224	0.91[ASN][1000 genomes]
rs2064226	0.87[ASN][1000 genomes]
rs2064227	0.91[ASN][1000 genomes]
rs2064230	0.84[ASN][1000 genomes]
rs2064231	0.81[ASN][1000 genomes]
rs2065857	0.82[ASN][1000 genomes]
rs2294698	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs2294706	0.89[CHB][hapmap]
rs2294709	0.89[CHB][hapmap]
rs2784871	0.80[ASN][1000 genomes]
rs2784872	0.87[ASN][1000 genomes]
rs2784875	0.87[ASN][1000 genomes]
rs3857503	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4263561	0.91[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4709713	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4709714	0.85[ASN][1000 genomes]
rs4709716	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs4709717	0.89[CHB][hapmap]
rs6455897	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6908317	0.87[ASN][1000 genomes]
rs6921172	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6927805	0.87[ASN][1000 genomes]
rs6929436	0.86[ASN][1000 genomes]
rs6939218	0.84[CHB][hapmap];0.90[JPT][hapmap]
rs715020	0.84[CHB][hapmap]
rs718878	0.85[ASN][1000 genomes]
rs718879	0.85[ASN][1000 genomes]
rs7772756	0.81[JPT][hapmap]
rs9346960	0.89[CHB][hapmap]
rs9347760	0.84[CHB][hapmap]
rs9364687	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9364689	0.89[CHB][hapmap]
rs9364691	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs9364692	0.89[CHB][hapmap]

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	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1022610	chr6:163591786-163814041	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv534621	chr6:163731741-163950870	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163791000-163813000	Weak transcription	Right Atrium	heart
2	chr6:163800800-163803600	Weak transcription	Spleen	Spleen
3	chr6:163802200-163802600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:163802200-163802600	Enhancers	Fetal Muscle Trunk	muscle
5	chr6:163802200-163802800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:163802200-163802800	Enhancers	Brain Anterior Caudate	brain
7	chr6:163802400-163802600	Enhancers	Fetal Muscle Leg	muscle
8	chr6:163802400-163802600	Flanking Active TSS	HepG2	liver
9	chr6:163802400-163802800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:163802400-163802800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:163802400-163802800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr6:163802400-163802800	Enhancers	Brain Cingulate Gyrus	brain
13	chr6:163802400-163803000	Enhancers	Brain Hippocampus Middle	brain
14	chr6:163802400-163803000	Enhancers	Brain Substantia Nigra	brain
15	chr6:163802400-163803200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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