Variant report

Variant	rs35701811
Chromosome Location	chr7:146976192-146976193
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs13221013	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13224375	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13242774	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13243107	0.90[EUR][1000 genomes]
rs1467329	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1467330	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17409790	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34166730	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34640787	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35018500	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35538572	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35827268	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36011986	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36074712	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62485027	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62485028	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62485029	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62485030	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62485031	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62485032	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62485034	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62485036	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62485038	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933033	chr7:146720301-147081560	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1033898	chr7:146721499-147081768	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv889396	chr7:146854133-147035067	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	esv33975	chr7:146968440-146991336	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146974200-146976600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr7:146974400-146976600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:146974400-146976800	Weak transcription	Brain Anterior Caudate	brain
4	chr7:146974800-146976800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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Input of quick search could be:

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

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