Variant report

Variant	rs34383892
Chromosome Location	chr4:97495951-97495952
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs13126115	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17025643	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17025657	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17446338	0.90[AMR][1000 genomes]
rs34849264	0.85[EUR][1000 genomes]
rs35565557	0.85[EUR][1000 genomes]
rs4699511	0.90[AMR][1000 genomes]
rs71605122	0.85[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	nsv879634	chr4:97371381-97727113	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv879635	chr4:97389090-97591085	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:97486000-97505000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:97495400-97496800	Enhancers	Dnd41	blood
3	chr4:97495600-97496600	Enhancers	Cortex derived primary cultured neurospheres	brain

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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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