Variant report

Variant	rs35871234
Chromosome Location	chr3:60835863-60835864
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:22)

rs_ID	r²[population]
rs10510855	0.91[EUR][1000 genomes]
rs13088848	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1839068	0.89[EUR][1000 genomes]
rs1839069	0.84[EUR][1000 genomes]
rs1947159	0.92[EUR][1000 genomes]
rs1947160	0.92[EUR][1000 genomes]
rs2100152	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2142297	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2205354	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2223084	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2250114	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2594132	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2594133	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2594136	0.89[EUR][1000 genomes]
rs2736748	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2736750	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2736751	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2736752	0.95[EUR][1000 genomes]
rs2736753	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34696953	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4974235	0.92[EUR][1000 genomes]
rs67917562	0.93[AMR][1000 genomes];0.97[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	nsv534038	chr3:60781917-60993082	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2757872	chr3:60781943-61019003	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2759152	chr3:60781943-61220809	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60833800-60839800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr3:60835400-60836000	Enhancers	Aorta	Aorta
3	chr3:60835600-60836200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr3:60835600-60836400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

Quick Search:

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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