Variant report

Variant	rs73326672
Chromosome Location	chr14:81023517-81023518
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10133617	1.00[EUR][1000 genomes]
rs10136245	1.00[EUR][1000 genomes]
rs10137925	1.00[EUR][1000 genomes]
rs10140445	1.00[EUR][1000 genomes]
rs10144134	1.00[EUR][1000 genomes]
rs10151108	1.00[EUR][1000 genomes]
rs10220319	1.00[EUR][1000 genomes]
rs1375628	1.00[EUR][1000 genomes]
rs17110847	1.00[EUR][1000 genomes]
rs17111025	1.00[EUR][1000 genomes]
rs2197983	1.00[EUR][1000 genomes]
rs327437	1.00[EUR][1000 genomes]
rs56933416	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57834417	1.00[EUR][1000 genomes]
rs58268321	1.00[EUR][1000 genomes]
rs58595334	1.00[EUR][1000 genomes]
rs60207137	1.00[EUR][1000 genomes]
rs61435414	1.00[EUR][1000 genomes]
rs73326644	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73328649	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73328655	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73328682	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73330508	1.00[EUR][1000 genomes]
rs73330519	1.00[AMR][1000 genomes]
rs73330520	1.00[AMR][1000 genomes]
rs73330543	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73332696	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73334792	1.00[EUR][1000 genomes]
rs73336577	1.00[EUR][1000 genomes]
rs73336590	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73336591	1.00[EUR][1000 genomes]
rs73336597	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73338970	1.00[EUR][1000 genomes]
rs73338973	1.00[EUR][1000 genomes]
rs73340517	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73340530	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73342506	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74064297	1.00[EUR][1000 genomes]
rs8020092	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	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv902116	chr14:81018237-81082400	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81013200-81023800	Weak transcription	Dnd41	blood
2	chr14:81021800-81025400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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