Variant report

Variant	rs73013393
Chromosome Location	chr2:168458362-168458363
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10209128	0.95[ASN][1000 genomes]
rs13384540	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13400955	1.00[AMR][1000 genomes]
rs13408596	0.95[ASN][1000 genomes]
rs13422865	0.90[ASN][1000 genomes]
rs1730727	0.86[ASN][1000 genomes]
rs73013384	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015406	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015407	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015412	0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491872	chr2:168220323-168737986	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv834449	chr2:168340043-168511856	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv583592	chr2:168356232-168721539	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3373785	chr2:168454206-168458804	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168452600-168463400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:168456200-168458600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
3	chr2:168458000-168458400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:168458200-168459600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell

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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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