Variant report

Variant	rs6656810
Chromosome Location	chr1:173584481-173584482
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10082296	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10128064	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10158274	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10159349	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12239406	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13313018	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13374735	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13375569	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13376081	1.00[AMR][1000 genomes]
rs13376339	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13376392	1.00[AMR][1000 genomes]
rs13376447	1.00[AMR][1000 genomes]
rs34683148	1.00[AMR][1000 genomes]
rs35052032	1.00[AMR][1000 genomes]
rs35133735	1.00[AMR][1000 genomes]
rs6425252	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6665497	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6695916	1.00[AMR][1000 genomes]
rs6703355	1.00[AMR][1000 genomes]
rs7349122	1.00[AMR][1000 genomes]
rs7518933	1.00[AMR][1000 genomes]
rs7532991	1.00[AMR][1000 genomes]
rs7540898	1.00[AMR][1000 genomes]
rs9286893	1.00[AMR][1000 genomes]
rs9425412	1.00[AMR][1000 genomes]
rs9425417	1.00[AMR][1000 genomes]
rs9425429	1.00[AMR][1000 genomes]
rs9425732	1.00[AMR][1000 genomes]
rs9425733	1.00[AMR][1000 genomes]
rs9425737	1.00[AMR][1000 genomes]
rs9425739	1.00[AMR][1000 genomes]
rs9425743	1.00[AMR][1000 genomes]
rs9425744	1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:173573400-173586000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr1:173582600-173586400	Weak transcription	iPS DF 19.11 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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