Variant report

Variant	rs6439843
Chromosome Location	chr3:138985699-138985700
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11921822	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1602630	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1602631	0.94[ASN][1000 genomes]
rs1948400	0.94[ASN][1000 genomes]
rs2068672	0.96[EUR][1000 genomes]
rs6439841	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6439842	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6439844	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7635629	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005167	chr3:138854490-138988546	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv536728	chr3:138854490-138988546	Enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138980000-138985800	Weak transcription	Spleen	Spleen
2	chr3:138984400-138986000	Weak transcription	Left Ventricle	heart
3	chr3:138984400-138986000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr3:138984600-138986200	Weak transcription	Brain Anterior Caudate	brain
5	chr3:138984800-138986200	Weak transcription	Ovary	ovary
6	chr3:138985200-138988200	Enhancers	Liver	Liver
7	chr3:138985400-138987000	Enhancers	Pancreas	Pancrea
8	chr3:138985600-138987000	Enhancers	Right Ventricle	heart

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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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