Variant report

Variant	rs72984357
Chromosome Location	chr6:142984905-142984906
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10484589	0.83[EUR][1000 genomes]
rs11968407	0.83[EUR][1000 genomes]
rs12663303	0.83[EUR][1000 genomes]
rs17071903	0.83[EUR][1000 genomes]
rs17071909	0.83[EUR][1000 genomes]
rs1876844	0.83[EUR][1000 genomes]
rs2136518	0.83[EUR][1000 genomes]
rs2136519	0.83[EUR][1000 genomes]
rs2175164	0.83[EUR][1000 genomes]
rs55671842	0.83[EUR][1000 genomes]
rs55702719	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55747254	0.83[EUR][1000 genomes]
rs55749277	0.83[EUR][1000 genomes]
rs55767236	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55787572	0.83[EUR][1000 genomes]
rs55889677	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56017506	0.83[EUR][1000 genomes]
rs56019737	0.83[EUR][1000 genomes]
rs56043044	0.83[EUR][1000 genomes]
rs56049518	0.83[EUR][1000 genomes]
rs56055844	0.83[EUR][1000 genomes]
rs56082312	0.83[EUR][1000 genomes]
rs56135811	0.83[EUR][1000 genomes]
rs56196468	0.83[EUR][1000 genomes]
rs56216981	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56228013	0.83[EUR][1000 genomes]
rs56267414	0.83[EUR][1000 genomes]
rs56358606	0.83[EUR][1000 genomes]
rs56363136	0.83[EUR][1000 genomes]
rs72982458	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72982478	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72984344	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72984346	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72996359	0.83[EUR][1000 genomes]
rs72996364	0.83[EUR][1000 genomes]
rs72998326	0.83[EUR][1000 genomes]
rs72998327	0.83[EUR][1000 genomes]
rs72998328	0.83[EUR][1000 genomes]
rs72998329	0.83[EUR][1000 genomes]
rs72998335	0.83[EUR][1000 genomes]
rs72998337	0.83[EUR][1000 genomes]
rs72998353	0.83[EUR][1000 genomes]
rs72998356	0.83[EUR][1000 genomes]
rs72998364	0.83[EUR][1000 genomes]
rs72998367	0.83[EUR][1000 genomes]
rs72998369	0.83[EUR][1000 genomes]
rs72998371	0.83[EUR][1000 genomes]
rs72998375	0.83[EUR][1000 genomes]
rs72998382	0.83[EUR][1000 genomes]
rs72998384	0.83[EUR][1000 genomes]
rs72998386	0.83[EUR][1000 genomes]
rs72998391	0.83[EUR][1000 genomes]
rs72998393	0.83[EUR][1000 genomes]
rs72998399	0.83[EUR][1000 genomes]
rs72998400	0.83[EUR][1000 genomes]
rs72998402	0.83[EUR][1000 genomes]
rs7759477	0.83[EUR][1000 genomes]
rs7772506	0.83[EUR][1000 genomes]
rs9376698	0.83[EUR][1000 genomes]

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	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv830827	chr6:142840734-143015005	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv830828	chr6:142970134-143116517	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142984200-142988200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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