Variant report

Variant	rs73347926
Chromosome Location	chr14:81462334-81462335
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11844944	1.00[EUR][1000 genomes]
rs11851120	1.00[EUR][1000 genomes]
rs13379243	1.00[EUR][1000 genomes]
rs28750114	1.00[EUR][1000 genomes]
rs58040173	1.00[AMR][1000 genomes]
rs58133007	1.00[AMR][1000 genomes]
rs58679489	1.00[AMR][1000 genomes]
rs60977678	1.00[AMR][1000 genomes]
rs73334006	1.00[AMR][1000 genomes]
rs73338189	1.00[AMR][1000 genomes]
rs73338199	1.00[AMR][1000 genomes]
rs73338226	1.00[AMR][1000 genomes]
rs73338235	1.00[AMR][1000 genomes]
rs73338237	1.00[AMR][1000 genomes]
rs73338251	1.00[AMR][1000 genomes]
rs73340105	1.00[AMR][1000 genomes]
rs73340175	1.00[AMR][1000 genomes]
rs73342195	1.00[AMR][1000 genomes]
rs73342245	1.00[AMR][1000 genomes]
rs73342273	1.00[AMR][1000 genomes]
rs73344031	1.00[AMR][1000 genomes]
rs73344062	1.00[AMR][1000 genomes]
rs73344072	1.00[AMR][1000 genomes]
rs73344073	1.00[AMR][1000 genomes]
rs73344075	1.00[AMR][1000 genomes]
rs73344078	1.00[AMR][1000 genomes]
rs73344096	1.00[AMR][1000 genomes]
rs73346054	1.00[AMR][1000 genomes]
rs73347933	1.00[EUR][1000 genomes]
rs73347935	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73347938	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73347947	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73347973	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73349940	1.00[EUR][1000 genomes]
rs8007755	1.00[EUR][1000 genomes]
rs8008523	1.00[EUR][1000 genomes]
rs8012937	1.00[EUR][1000 genomes]
rs8013119	1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81455400-81463800	Weak transcription	Thymus	Thymus
2	chr14:81455800-81492200	Weak transcription	Fetal Thymus	thymus
3	chr14:81459400-81465600	Strong transcription	Dnd41	blood
4	chr14:81459800-81462400	Weak transcription	Liver	Liver
5	chr14:81460600-81462600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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