Variant report

Variant	rs7623704
Chromosome Location	chr3:21063888-21063889
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs13097458	0.91[ASN][1000 genomes]
rs1391138	0.91[ASN][1000 genomes]
rs1497516	0.93[ASN][1000 genomes]
rs4306882	0.93[ASN][1000 genomes]
rs4431129	0.93[ASN][1000 genomes]
rs4431130	0.93[ASN][1000 genomes]
rs4465961	0.90[ASN][1000 genomes]
rs4858288	0.91[ASN][1000 genomes]
rs6550561	0.90[ASN][1000 genomes]
rs7612422	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7625772	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs7633632	0.93[ASN][1000 genomes]
rs7652147	0.91[ASN][1000 genomes]
rs869494	0.93[ASN][1000 genomes]
rs869495	0.93[ASN][1000 genomes]
rs973870	0.91[ASN][1000 genomes]
rs9811079	0.91[ASN][1000 genomes]
rs9881998	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876607	chr3:20972475-21087219	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
2	nsv876608	chr3:21008710-21203048	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv998068	chr3:21050191-21212603	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21059000-21065800	Weak transcription	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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