Variant report

Variant	rs9681520
Chromosome Location	chr3:68790938-68790939
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11128087	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1504297	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1602195	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2221394	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2313851	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4855498	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4855499	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6549141	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6775453	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6795777	0.85[EUR][1000 genomes]
rs6796615	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs867310	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9682904	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs971382	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9836496	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9841811	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[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	nsv834722	chr3:68775036-68974120	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68789400-68801200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:68790600-68791400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:68790600-68795400	Enhancers	Primary hematopoietic stem cells	blood

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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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