Variant report

Variant	rs12030394
Chromosome Location	chr1:195715978-195715979
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10494729	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10921905	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11807635	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11807832	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11810167	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12029946	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12030830	0.82[ASN][1000 genomes]
rs12034483	0.82[ASN][1000 genomes]
rs12037920	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12038958	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12042500	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12042815	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12045875	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12046609	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12048401	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12073625	0.85[EUR][1000 genomes]
rs12073662	0.87[EUR][1000 genomes]
rs2104875	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs60298660	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs66471251	0.87[EUR][1000 genomes]
rs72734141	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72734147	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72734167	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72736123	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72736141	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72736142	0.85[EUR][1000 genomes]
rs876716	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][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	chr1:195715000-195718400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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