Variant report

Variant	rs1856443
Chromosome Location	chr6:126744924-126744925
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs34929677	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41324148	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57255415	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57539450	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57823858	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61069279	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61360672	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9491569	1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:126744000-126749000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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