Variant report

Variant	rs2610884
Chromosome Location	chr10:55750941-55750942
allele	A/C
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:15)

rs_ID	r²[population]
rs11003968	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11003996	0.95[ASN][1000 genomes]
rs12570313	0.80[ASN][1000 genomes]
rs12571668	0.82[ASN][1000 genomes]
rs12572470	0.80[ASN][1000 genomes]
rs2253198	0.96[ASN][1000 genomes]
rs2456701	0.80[ASN][1000 genomes]
rs2593131	0.80[ASN][1000 genomes]
rs2610885	0.89[ASN][1000 genomes]
rs2660147	0.90[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2660180	0.96[ASN][1000 genomes]
rs2660188	0.80[ASN][1000 genomes]
rs2660190	0.80[ASN][1000 genomes]
rs2926405	0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2926406	1.00[AMR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949692	chr10:55502542-55893206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1052939	chr10:55654719-55769239	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv869303	chr10:55714219-55857931	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	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	chr10:55750400-55751000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
2	chr10:55750400-55751200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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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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