Variant report

Variant	rs6826195
Chromosome Location	chr4:81313620-81313621
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1039051	0.90[AFR][1000 genomes]
rs12642262	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1495483	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1495485	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1495488	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2007145	0.83[AMR][1000 genomes]
rs4693021	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4693100	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4693384	0.83[AMR][1000 genomes]
rs4693688	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6534890	0.83[AMR][1000 genomes]
rs7665080	0.81[AFR][1000 genomes]
rs7691290	0.81[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81308200-81314800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr4:81308600-81314600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:81311200-81314000	Weak transcription	Osteobl	bone

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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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