Variant report

Variant	rs73322215
Chromosome Location	chr14:78652319-78652320
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs12885580	0.88[ASN][1000 genomes]
rs17107006	1.00[AMR][1000 genomes]
rs17107009	1.00[AMR][1000 genomes]
rs17107117	0.93[ASN][1000 genomes]
rs28542174	1.00[AMR][1000 genomes]
rs28731105	1.00[AMR][1000 genomes]
rs4312244	0.93[ASN][1000 genomes]
rs57617792	0.91[ASN][1000 genomes]
rs57679658	0.93[ASN][1000 genomes]
rs59184512	1.00[AMR][1000 genomes]
rs59583601	0.91[ASN][1000 genomes]
rs59857748	0.93[ASN][1000 genomes]
rs60137667	0.82[ASN][1000 genomes]
rs60156450	0.93[ASN][1000 genomes]
rs60410935	0.93[ASN][1000 genomes]
rs60502805	0.91[ASN][1000 genomes]
rs60973131	0.93[ASN][1000 genomes]
rs73308584	1.00[AMR][1000 genomes]
rs73308593	1.00[AMR][1000 genomes]
rs73310308	1.00[AMR][1000 genomes]
rs73316330	1.00[AMR][1000 genomes]
rs73316332	1.00[AMR][1000 genomes]
rs73316335	1.00[AMR][1000 genomes]
rs73316341	1.00[AMR][1000 genomes]
rs73316342	1.00[AMR][1000 genomes]
rs73316345	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316348	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316357	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316362	1.00[AMR][1000 genomes]
rs73316371	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316373	1.00[AMR][1000 genomes]
rs73316375	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316376	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73322213	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1366	chr14:78633044-78677718	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv1038627	chr14:78635498-78657912	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78648000-78659000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:78649000-78652600	Enhancers	Brain Germinal Matrix	brain
3	chr14:78651600-78654600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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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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