Variant report

Variant	rs10089172
Chromosome Location	chr8:91668625-91668626
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10099433	0.88[AMR][1000 genomes]
rs10101451	0.86[YRI][hapmap];0.82[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs10103441	1.00[YRI][hapmap]
rs16905097	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28480323	0.82[AMR][1000 genomes]
rs28517725	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28521858	0.83[AMR][1000 genomes]
rs28523907	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28533479	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs28716641	0.89[AMR][1000 genomes]
rs4513931	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4588812	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58636900	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73694518	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91666800-91677800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:91667600-91669200	ZNF genes & repeats	hESC Derived CD184+ Endoderm 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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