Variant report

Variant	rs34065209
Chromosome Location	chr1:102058640-102058641
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10493957	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10493958	0.97[EUR][1000 genomes]
rs11164238	0.97[EUR][1000 genomes]
rs11164239	0.97[EUR][1000 genomes]
rs11164241	0.97[EUR][1000 genomes]
rs11164243	0.97[EUR][1000 genomes]
rs11164244	0.97[EUR][1000 genomes]
rs11164245	0.97[EUR][1000 genomes]
rs11164247	0.97[EUR][1000 genomes]
rs11164250	0.91[EUR][1000 genomes]
rs11164251	0.91[EUR][1000 genomes]
rs11164252	0.91[EUR][1000 genomes]
rs11488027	0.97[EUR][1000 genomes]
rs12068247	0.97[EUR][1000 genomes]
rs12068329	0.97[EUR][1000 genomes]
rs12073459	0.97[EUR][1000 genomes]
rs12073466	0.97[EUR][1000 genomes]
rs12074035	0.97[EUR][1000 genomes]
rs12074808	0.97[EUR][1000 genomes]
rs12078720	0.97[EUR][1000 genomes]
rs12078847	0.97[EUR][1000 genomes]
rs12079908	0.97[EUR][1000 genomes]
rs12080001	0.97[EUR][1000 genomes]
rs12083840	0.91[EUR][1000 genomes]
rs12088445	0.97[EUR][1000 genomes]
rs12088450	0.97[EUR][1000 genomes]
rs12094579	0.97[EUR][1000 genomes]
rs12724739	0.97[EUR][1000 genomes]
rs12728472	0.91[EUR][1000 genomes]
rs12729855	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12743322	0.97[EUR][1000 genomes]
rs1484295	0.97[EUR][1000 genomes]
rs1484296	0.97[EUR][1000 genomes]
rs1484303	0.91[EUR][1000 genomes]
rs17125096	0.97[EUR][1000 genomes]
rs17125156	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17125161	0.94[EUR][1000 genomes]
rs28772944	0.97[EUR][1000 genomes]
rs28786227	0.97[EUR][1000 genomes]
rs28789110	0.91[EUR][1000 genomes]
rs28790366	0.97[EUR][1000 genomes]
rs28822436	0.97[EUR][1000 genomes]
rs28893919	0.97[EUR][1000 genomes]
rs35628451	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35681286	0.91[EUR][1000 genomes]
rs55661599	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55994851	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs66943779	0.97[EUR][1000 genomes]
rs67789472	0.97[EUR][1000 genomes]
rs72978678	0.97[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830848	chr1:101930303-102114220	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	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	chr1:102058400-102058800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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