Variant report

Variant	rs4917095
Chromosome Location	chr7:49909953-49909954
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs11185592	0.90[ASN][1000 genomes]
rs11185593	0.90[ASN][1000 genomes]
rs11978548	0.86[ASN][1000 genomes]
rs12532827	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12718225	0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs13245999	0.91[ASN][1000 genomes]
rs1351694	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1384635	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1384636	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1384637	0.90[ASN][1000 genomes]
rs1483071	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1483072	0.90[ASN][1000 genomes]
rs1483074	0.88[ASN][1000 genomes]
rs1483084	0.86[ASN][1000 genomes]
rs1483094	0.86[ASN][1000 genomes]
rs1564740	0.90[ASN][1000 genomes]
rs1567269	0.90[ASN][1000 genomes]
rs1872137	0.90[ASN][1000 genomes]
rs1911765	0.86[ASN][1000 genomes]
rs1983159	0.86[ASN][1000 genomes]
rs1983162	0.86[ASN][1000 genomes]
rs2046300	0.86[ASN][1000 genomes]
rs2086696	0.86[ASN][1000 genomes]
rs2170787	0.90[ASN][1000 genomes]
rs2365784	0.86[ASN][1000 genomes]
rs2886462	0.86[ASN][1000 genomes]
rs3850669	0.86[ASN][1000 genomes]
rs4451253	0.90[ASN][1000 genomes]
rs4916995	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4916997	0.90[ASN][1000 genomes]
rs4916998	0.90[ASN][1000 genomes]
rs4917094	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs495813	0.91[ASN][1000 genomes]
rs539930	0.90[ASN][1000 genomes]
rs598871	0.90[ASN][1000 genomes]
rs623107	0.90[ASN][1000 genomes]
rs6583394	0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6583395	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6583396	0.90[ASN][1000 genomes]
rs6583397	0.90[ASN][1000 genomes]
rs690842	0.98[ASN][1000 genomes]
rs691194	0.98[ASN][1000 genomes]
rs691458	0.90[ASN][1000 genomes]
rs691636	0.81[ASN][1000 genomes]
rs692039	0.98[ASN][1000 genomes]
rs692201	0.90[ASN][1000 genomes]
rs6952121	0.98[ASN][1000 genomes]
rs6953702	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6957719	0.90[ASN][1000 genomes]
rs6963083	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6966640	0.91[ASN][1000 genomes]
rs6977361	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs726383	0.86[ASN][1000 genomes]
rs769922	0.90[ASN][1000 genomes]
rs7779095	0.90[ASN][1000 genomes]
rs7797267	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7802037	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7809987	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs985489	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464444	chr7:49671882-50454736	Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv606897	chr7:49671883-50454736	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv498090	chr7:49708644-50427714	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1020869	chr7:49712860-50457544	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:49906600-49915000	Weak transcription	Ovary	ovary
2	chr7:49906800-49917800	Weak transcription	Fetal Heart	heart
3	chr7:49907200-49914800	Weak transcription	Right Ventricle	heart
4	chr7:49907200-49915000	Weak transcription	Pancreas	Pancrea
5	chr7:49907400-49915000	Weak transcription	Left Ventricle	heart

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