Variant report

Variant	rs10222179
Chromosome Location	chr21:15969689-15969690
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11909109	1.00[EUR][1000 genomes]
rs17003822	1.00[EUR][1000 genomes]
rs17003830	1.00[EUR][1000 genomes]
rs17003835	1.00[EUR][1000 genomes]
rs17003879	1.00[EUR][1000 genomes]
rs55660680	1.00[EUR][1000 genomes]
rs56315338	1.00[EUR][1000 genomes]
rs57281261	1.00[EUR][1000 genomes]
rs57369522	1.00[EUR][1000 genomes]
rs58711927	1.00[EUR][1000 genomes]
rs59115274	1.00[EUR][1000 genomes]
rs59489313	1.00[EUR][1000 genomes]
rs60481541	1.00[EUR][1000 genomes]
rs60792477	1.00[EUR][1000 genomes]
rs6516924	1.00[EUR][1000 genomes]
rs7276028	1.00[EUR][1000 genomes]
rs73894114	1.00[EUR][1000 genomes]
rs73894115	1.00[EUR][1000 genomes]
rs73894119	1.00[EUR][1000 genomes]
rs73894121	1.00[EUR][1000 genomes]
rs73894153	1.00[EUR][1000 genomes]
rs73894154	1.00[EUR][1000 genomes]
rs73894155	1.00[EUR][1000 genomes]
rs73894178	1.00[EUR][1000 genomes]
rs73894180	1.00[EUR][1000 genomes]
rs73894185	1.00[EUR][1000 genomes]
rs8128543	1.00[EUR][1000 genomes]
rs8129135	1.00[EUR][1000 genomes]
rs8129964	1.00[EUR][1000 genomes]
rs8131281	1.00[EUR][1000 genomes]
rs9305396	0.85[AFR][1000 genomes];1.00[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	nsv834045	chr21:15900678-16112850	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv834046	chr21:15903792-16077369	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15965000-15970800	Weak transcription	Fetal Lung	lung
2	chr21:15966800-15970000	Weak transcription	Fetal Stomach	stomach
3	chr21:15969200-15972200	Weak transcription	K562	blood
4	chr21:15969200-15975000	Weak transcription	H9 Cell Line	embryonic stem cell

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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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