Variant report

Variant	rs1207167
Chromosome Location	chr6:71837449-71837450
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1739803	1.00[AMR][1000 genomes]
rs1739804	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1819738	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1891524	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1935804	1.00[AMR][1000 genomes]
rs1935805	1.00[AMR][1000 genomes]
rs2881839	1.00[AMR][1000 genomes]
rs58530565	1.00[AMR][1000 genomes]
rs73500913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73501153	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73501157	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7743246	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455331	1.00[AMR][1000 genomes]
rs9455333	1.00[AMR][1000 genomes]
rs9455340	1.00[AFR][1000 genomes];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	chr6:71834600-71848800	Weak transcription	NH-A	brain
2	chr6:71837000-71837600	Enhancers	Primary neutrophils fromperipheralblood	blood

Quick Search:

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

what's new

Quick links