Variant report

Variant	rs73056370
Chromosome Location	chr1:195693981-195693982
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10218650	1.00[EUR][1000 genomes]
rs10218674	1.00[EUR][1000 genomes]
rs28893320	1.00[EUR][1000 genomes]
rs56300618	1.00[EUR][1000 genomes]
rs57057259	0.95[AFR][1000 genomes]
rs57268177	1.00[EUR][1000 genomes]
rs57446733	1.00[EUR][1000 genomes]
rs57535547	1.00[EUR][1000 genomes]
rs60001488	1.00[EUR][1000 genomes]
rs61137731	1.00[EUR][1000 genomes]
rs6676487	1.00[EUR][1000 genomes]
rs6687918	1.00[EUR][1000 genomes]
rs73056346	0.83[AFR][1000 genomes]
rs73056348	0.86[AFR][1000 genomes]
rs73056357	0.90[AFR][1000 genomes]
rs73056369	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73060574	1.00[EUR][1000 genomes]
rs7512397	1.00[EUR][1000 genomes]
rs7524605	1.00[EUR][1000 genomes]
rs7524894	1.00[EUR][1000 genomes]
rs7533420	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872894	chr1:195053221-195745968	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1009307	chr1:195368381-195726703	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv872932	chr1:195447286-195736070	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv872937	chr1:195493538-195849028	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1007203	chr1:195672857-195902360	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:195693400-195699200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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