Variant report

Variant	rs73324228
Chromosome Location	chr7:48630225-48630226
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10265163	0.83[EUR][1000 genomes]
rs17132372	0.88[EUR][1000 genomes]
rs17132432	1.00[EUR][1000 genomes]
rs17132434	1.00[EUR][1000 genomes]
rs17132444	1.00[EUR][1000 genomes]
rs17132457	1.00[EUR][1000 genomes]
rs17132463	1.00[EUR][1000 genomes]
rs17132508	0.85[EUR][1000 genomes]
rs41523451	1.00[EUR][1000 genomes]
rs4606009	0.85[EUR][1000 genomes]
rs55651521	0.85[EUR][1000 genomes]
rs56093045	0.88[EUR][1000 genomes]
rs58385535	0.88[EUR][1000 genomes]
rs59965341	1.00[EUR][1000 genomes]
rs60694997	0.88[EUR][1000 genomes]
rs61346153	0.88[EUR][1000 genomes]
rs61451174	0.88[EUR][1000 genomes]
rs6951282	1.00[EUR][1000 genomes]
rs6960177	0.88[EUR][1000 genomes]
rs6971823	1.00[EUR][1000 genomes]
rs73324231	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73694635	0.80[EUR][1000 genomes]
rs73694639	0.88[EUR][1000 genomes]
rs73694640	0.88[EUR][1000 genomes]
rs73694648	0.93[EUR][1000 genomes]
rs73694650	0.93[EUR][1000 genomes]
rs73694653	0.90[EUR][1000 genomes]
rs73694656	0.90[EUR][1000 genomes]
rs73694659	1.00[EUR][1000 genomes]
rs73694660	1.00[EUR][1000 genomes]
rs73694665	1.00[EUR][1000 genomes]
rs73694667	1.00[EUR][1000 genomes]
rs73694668	1.00[EUR][1000 genomes]
rs73694670	1.00[EUR][1000 genomes]
rs73694671	1.00[EUR][1000 genomes]
rs73694678	1.00[EUR][1000 genomes]
rs73694693	0.80[EUR][1000 genomes]
rs73694694	0.85[EUR][1000 genomes]
rs73694695	0.85[EUR][1000 genomes]
rs7793028	1.00[EUR][1000 genomes]
rs7801591	0.85[EUR][1000 genomes]
rs7812121	0.85[EUR][1000 genomes]
rs9969343	1.00[EUR][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	nsv830992	chr7:48497408-48686442	Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases
2	nsv888008	chr7:48568425-48652224	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48600400-48634200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:48630200-48634000	Weak transcription	Primary neutrophils 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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