Variant report

Variant	rs34602668
Chromosome Location	chr5:113308848-113308849
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1386465	0.81[EUR][1000 genomes]
rs1386467	0.89[EUR][1000 genomes]
rs1482486	0.89[EUR][1000 genomes]
rs17136157	0.89[EUR][1000 genomes]
rs17136163	0.89[EUR][1000 genomes]
rs17136164	0.89[EUR][1000 genomes]
rs17136167	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2054842	1.00[EUR][1000 genomes]
rs60594126	0.89[EUR][1000 genomes]
rs6875841	0.89[EUR][1000 genomes]
rs6888149	0.81[EUR][1000 genomes]
rs73254466	0.89[EUR][1000 genomes]
rs73254474	0.82[EUR][1000 genomes]
rs73254486	0.89[EUR][1000 genomes]
rs73779591	0.89[EUR][1000 genomes]
rs73779593	0.89[EUR][1000 genomes]
rs9968734	0.89[EUR][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	nsv471042	chr5:113160490-113440892	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv980714	chr5:113301277-113321673	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113307400-113310600	Weak transcription	Fetal Heart	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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