Variant report

Variant	rs10958916
Chromosome Location	chr9:10146196-10146197
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10809027	0.90[JPT][hapmap]
rs10958888	0.81[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs10958889	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs10958890	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs10958891	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs10958892	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs10958894	0.81[ASN][1000 genomes]
rs10958895	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs10958896	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs10958897	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs10958898	0.91[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs10958899	0.90[CHB][hapmap]
rs10958900	0.90[CHB][hapmap]
rs10958901	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs10958902	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs10958904	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs10958905	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs10958906	0.91[CHB][hapmap]
rs10958907	0.90[CHB][hapmap]
rs10958909	0.90[CHB][hapmap]
rs10958910	0.90[CHB][hapmap]
rs10958911	0.90[CHB][hapmap]
rs10958917	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12004515	0.91[JPT][hapmap]
rs12235311	1.00[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs12235475	0.80[CHB][hapmap]
rs12553060	0.91[CHB][hapmap]
rs12555583	0.89[CHB][hapmap];0.81[JPT][hapmap]
rs1304641	0.90[CHB][hapmap]
rs1322159	0.90[CHB][hapmap]
rs1322160	0.91[CHB][hapmap]
rs1567404	0.90[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs1575260	0.91[CHB][hapmap]
rs16931167	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs16931219	0.90[CHB][hapmap]
rs2382105	0.89[CHB][hapmap]
rs2382107	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs2382195	0.91[CHB][hapmap]
rs4629932	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs4741010	0.81[ASN][1000 genomes]
rs58750073	0.81[ASN][1000 genomes]
rs66623460	0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs67224985	0.81[ASN][1000 genomes]
rs67926901	0.81[ASN][1000 genomes]
rs7037950	0.90[CHB][hapmap]
rs7043462	0.90[CHB][hapmap]
rs724231	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs725261	0.91[CHB][hapmap]
rs725262	0.90[CHB][hapmap]
rs7341885	0.91[CHB][hapmap];0.81[JPT][hapmap];0.81[ASN][1000 genomes]
rs7341924	0.91[CHB][hapmap];0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034731	chr9:9776126-10481262	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv892295	chr9:9832245-10380406	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv892302	chr9:9974221-10158866	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1030657	chr9:10002355-10481262	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv831506	chr9:10040172-10204609	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1024401	chr9:10105656-10218577	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv539995	chr9:10105656-10218577	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv466157	chr9:10119504-10170101	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	inside rSNPs	diseases
9	nsv613374	chr9:10119504-10170101	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	inside rSNPs	diseases
10	nsv892308	chr9:10139580-10178560	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:10145200-10146400	Enhancers	Liver	Liver
2	chr9:10145400-10146800	Weak transcription	Fetal Heart	heart

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