Variant report

Variant	rs10157476
Chromosome Location	chr8:64668856-64668857
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10733056	0.80[AFR][1000 genomes]
rs10753810	0.92[AFR][1000 genomes]
rs10753811	0.91[AFR][1000 genomes]
rs10919393	0.91[AFR][1000 genomes]
rs10919425	0.80[AFR][1000 genomes]
rs1333146	0.93[AFR][1000 genomes]
rs1333150	0.82[AFR][1000 genomes]
rs1333151	0.95[AFR][1000 genomes]
rs1333152	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1333153	0.95[AFR][1000 genomes]
rs1333154	0.95[AFR][1000 genomes]
rs1412891	0.93[AFR][1000 genomes]
rs1412894	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs1537395	0.93[AFR][1000 genomes]
rs1572026	0.95[AFR][1000 genomes]
rs1572027	0.93[AFR][1000 genomes]
rs1576980	0.80[AFR][1000 genomes]
rs1831756	0.95[AFR][1000 genomes]
rs1930633	0.95[AFR][1000 genomes]
rs1930634	0.95[AFR][1000 genomes]
rs2151333	0.92[AFR][1000 genomes]
rs2901401	0.80[AFR][1000 genomes]
rs3936919	0.93[AFR][1000 genomes]
rs3980839	0.82[AFR][1000 genomes]
rs4319388	0.85[AFR][1000 genomes]
rs4411178	0.89[AFR][1000 genomes]
rs4436439	0.91[AFR][1000 genomes]
rs4469769	0.95[AFR][1000 genomes]
rs4656771	0.93[AFR][1000 genomes]
rs4656779	0.80[AFR][1000 genomes]
rs4656783	0.81[AFR][1000 genomes]
rs6427255	0.95[AFR][1000 genomes]
rs6660575	0.81[AFR][1000 genomes]
rs6664037	0.82[AFR][1000 genomes]
rs6667304	0.83[AFR][1000 genomes]
rs6670724	0.80[AFR][1000 genomes]
rs6670882	0.82[AFR][1000 genomes]
rs6698637	0.92[AFR][1000 genomes]
rs6701004	0.95[AFR][1000 genomes]
rs6701218	0.81[AFR][1000 genomes]
rs9651042	0.92[AFR][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	nsv831344	chr8:64658229-64712338	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64666400-64671200	Weak transcription	GM12878-XiMat	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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