Variant report

Variant	rs6919939
Chromosome Location	chr6:164975014-164975015
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1021614	0.88[ASN][1000 genomes]
rs1391239	0.88[ASN][1000 genomes]
rs1497735	0.87[ASN][1000 genomes]
rs1603332	0.86[ASN][1000 genomes]
rs1909052	0.88[ASN][1000 genomes]
rs2019943	0.88[ASN][1000 genomes]
rs2132411	0.86[ASN][1000 genomes]
rs2201806	0.86[ASN][1000 genomes]
rs4709856	0.88[ASN][1000 genomes]
rs4709863	0.88[ASN][1000 genomes]
rs6920546	0.88[ASN][1000 genomes]
rs7760143	0.88[ASN][1000 genomes]
rs9295282	0.88[ASN][1000 genomes]
rs9347872	0.88[ASN][1000 genomes]
rs9365729	0.88[ASN][1000 genomes]
rs9459136	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs9459138	0.87[ASN][1000 genomes]
rs9918342	0.88[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	nsv1029952	chr6:164463355-165268911	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv886919	chr6:164756364-165079834	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv511924	chr6:164762179-165077399	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1016147	chr6:164765938-165046731	Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv886920	chr6:164931002-164980871	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv1018087	chr6:164938719-165048492	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1017076	chr6:164945167-165195092	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:164969000-164977600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:164972600-164976000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:164974600-164977000	Enhancers	Fetal Brain Male	brain
4	chr6:164975000-164975800	Enhancers	Fetal Brain Female	brain
5	chr6:164975000-164976000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr6:164975000-164976800	Enhancers	Brain Germinal Matrix	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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