Variant report

Variant	rs10459870
Chromosome Location	chr16:80429577-80429578
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:80427816..80429853-chr16:80431372..80434203,2	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10459869	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12443517	0.84[AMR][1000 genomes]
rs12444518	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12446534	0.90[ASN][1000 genomes]
rs12596682	0.89[ASN][1000 genomes]
rs12597207	0.89[ASN][1000 genomes]
rs12598715	0.81[AMR][1000 genomes]
rs12599990	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12600017	0.85[AMR][1000 genomes]
rs12716890	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12933734	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13334483	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1484029	0.80[ASN][1000 genomes]
rs16953259	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16953272	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16953274	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16953276	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16953280	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16953281	0.83[AMR][1000 genomes]
rs16953285	0.84[AMR][1000 genomes]
rs2129044	0.80[AFR][1000 genomes]
rs55896457	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55958632	0.84[AMR][1000 genomes]
rs60512064	0.81[ASN][1000 genomes]
rs62048557	0.91[ASN][1000 genomes]
rs62048559	0.91[ASN][1000 genomes]
rs62050388	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62050389	0.80[ASN][1000 genomes]
rs62050390	0.80[ASN][1000 genomes]
rs62050396	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62050397	0.84[AMR][1000 genomes]
rs62050422	0.84[AMR][1000 genomes]
rs62050423	0.84[AMR][1000 genomes]
rs7184383	0.81[AMR][1000 genomes]
rs7193865	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7194288	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7196055	0.91[ASN][1000 genomes]
rs7201564	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7202443	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8043750	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8047032	0.84[AMR][1000 genomes]
rs8052344	0.84[AMR][1000 genomes]
rs8053767	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8057483	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8057943	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8063777	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9925586	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9932786	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9972739	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061068	chr16:80207546-80537052	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv949197	chr16:80284557-80456403	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv2762333	chr16:80307755-80509983	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv1056026	chr16:80317627-80471469	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv542987	chr16:80317627-80471469	Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv833299	chr16:80341745-80549683	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1061190	chr16:80392009-80471330	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv542988	chr16:80392009-80471330	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv457557	chr16:80405292-80463399	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv573297	chr16:80405292-80463399	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv907000	chr16:80405292-80473018	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv907001	chr16:80405292-80620611	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80425200-80430600	Weak transcription	Fetal Kidney	kidney

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