Variant report

Variant	rs1164302
Chromosome Location	chr3:144377200-144377201
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1151554	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1151560	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1164303	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1178899	1.00[AFR][1000 genomes]
rs1178900	1.00[AFR][1000 genomes]
rs1178904	0.81[EUR][1000 genomes]
rs1178908	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1178910	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1178917	0.81[EUR][1000 genomes]
rs1405598	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs1527235	0.81[EUR][1000 genomes]
rs1726520	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs941213	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs941215	1.00[AMR][1000 genomes];1.00[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	nsv532633	chr3:143802417-144440646	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv591928	chr3:144050897-144822081	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv3379740	chr3:144225847-144433818	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv2757895	chr3:144236202-144391387	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv2759185	chr3:144236202-144391387	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 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	chr3:144377000-144378200	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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