Variant report

Variant	rs67870248
Chromosome Location	chr10:97733604-97733605
allele	A/G
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:12)

rs_ID	r²[population]
rs11599105	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12761082	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12762284	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12765198	0.86[EUR][1000 genomes]
rs12775584	0.93[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs34777055	0.93[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs35298116	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35864527	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs66530311	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs66851219	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67166869	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7904176	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761619	chr10:97719520-97746180	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97725400-97735800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr10:97725400-97736200	Weak transcription	GM12878-XiMat	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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