Variant report

Variant	rs4694835
Chromosome Location	chr4:47115201-47115202
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs13108870	0.80[EUR][1000 genomes]
rs13140672	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1442103	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1561778	0.84[AFR][1000 genomes]
rs34541375	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34552901	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34926350	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35839630	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs36002778	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4695191	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62305289	0.81[EUR][1000 genomes]
rs6447532	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67848491	0.88[AFR][1000 genomes]
rs6818828	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7686292	0.82[AMR][1000 genomes];0.81[EUR][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	nsv537078	chr4:47059778-47137372	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv829922	chr4:47093785-47261181	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv879003	chr4:47102993-47215939	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47114400-47120600	Weak transcription	Fetal Lung	lung
2	chr4:47115200-47120600	Weak transcription	Fetal Brain Male	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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