Variant report

Variant	rs73236929
Chromosome Location	chr5:118185887-118185888
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs57626866	0.87[AFR][1000 genomes]
rs58554745	1.00[EUR][1000 genomes]
rs59300139	1.00[EUR][1000 genomes]
rs60664847	1.00[EUR][1000 genomes]
rs60694838	1.00[EUR][1000 genomes]
rs61466105	1.00[EUR][1000 genomes]
rs73234487	1.00[EUR][1000 genomes]
rs73236933	1.00[EUR][1000 genomes]
rs73236935	1.00[EUR][1000 genomes]
rs73236937	1.00[EUR][1000 genomes]
rs73239060	1.00[EUR][1000 genomes]
rs73239063	1.00[EUR][1000 genomes]
rs73239075	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	nsv882767	chr5:117931730-118385691	Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv599562	chr5:118122504-118230640	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv882771	chr5:118170135-118230640	Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv882772	chr5:118173127-118230640	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv882773	chr5:118175640-118241854	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers 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	chr5:118167800-118186400	Weak transcription	Liver	Liver
2	chr5:118169600-118208600	Weak transcription	Aorta	Aorta
3	chr5:118172200-118188600	Weak transcription	Primary T cells from cord blood	blood
4	chr5:118175400-118186200	Weak transcription	Primary B cells from cord blood	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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