Variant report

Variant	rs6938579
Chromosome Location	chr6:164205230-164205231
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:164197060..164200042-chr6:164203079..164205559,3	K562	blood:

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10945921	1.00[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10945924	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1555229	0.81[CHB][hapmap];0.93[JPT][hapmap];0.83[ASN][1000 genomes]
rs16895332	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2321977	0.89[ASN][1000 genomes]
rs2321978	0.83[CEU][hapmap];0.86[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs2321979	0.86[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap];0.86[ASN][1000 genomes]
rs4709767	0.94[AFR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4709768	0.86[ASN][1000 genomes]
rs4709769	0.85[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs62435339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62435340	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62436876	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62436877	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62436878	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62436879	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6455921	0.96[AFR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6455922	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6914115	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6914628	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6934397	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6935481	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7740670	0.82[CEU][hapmap];0.81[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs7742306	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7759487	0.83[ASN][1000 genomes]
rs7765512	0.94[AFR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs876738	0.94[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs9295230	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9355441	0.86[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap];0.86[ASN][1000 genomes]
rs9365618	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9365622	0.83[ASN][1000 genomes]
rs9456886	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9458899	0.96[AFR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9458901	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[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	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1026707	chr6:164188210-164749206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv538527	chr6:164188210-164749206	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164200800-164209200	Weak transcription	Psoas Muscle	Psoas
2	chr6:164202400-164209400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr6:164202600-164209200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:164202800-164208000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:164203800-164208200	Weak transcription	K562	blood
6	chr6:164204000-164209200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr6:164204000-164210400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:164204000-164210600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr6:164204400-164209200	Weak transcription	Fetal Muscle Leg	muscle
10	chr6:164204400-164210200	Weak transcription	GM12878-XiMat	blood

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