Variant report

Variant	rs7023760
Chromosome Location	chr9:13881467-13881468
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10125418	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs10810045	0.90[ASN][1000 genomes]
rs10810050	0.90[ASN][1000 genomes]
rs10810055	0.90[ASN][1000 genomes]
rs10810057	1.00[CHB][hapmap]
rs10961291	1.00[JPT][hapmap]
rs10961297	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10961300	0.82[AMR][1000 genomes]
rs12002277	0.90[ASN][1000 genomes]
rs12006148	0.80[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs12344771	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12344958	0.90[ASN][1000 genomes]
rs12350449	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1373252	0.80[AMR][1000 genomes]
rs1410019	0.90[ASN][1000 genomes]
rs1410023	0.90[ASN][1000 genomes]
rs17822351	0.82[AMR][1000 genomes]
rs1822541	0.88[CEU][hapmap]
rs1822542	0.80[AMR][1000 genomes]
rs2382425	0.82[AMR][1000 genomes]
rs4548276	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6474794	1.00[JPT][hapmap]
rs7019911	0.81[AMR][1000 genomes]
rs7023898	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7024597	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7029494	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7031343	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7035288	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7035382	0.86[AMR][1000 genomes]
rs7036035	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7850903	0.83[AMR][1000 genomes]
rs7851314	0.83[AMR][1000 genomes]
rs7854416	0.83[AMR][1000 genomes]
rs7854918	0.82[AMR][1000 genomes]
rs7864043	0.81[AMR][1000 genomes]
rs7874643	0.90[ASN][1000 genomes]
rs7874825	0.90[ASN][1000 genomes]
rs981564	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9886719	0.90[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	nsv1022001	chr9:13717736-13983738	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer 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	nsv1033764	chr9:13764918-14226168	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1032113	chr9:13861066-13923136	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1032447	chr9:13861066-13923673	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 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	chr9:13863400-13884200	Weak transcription	Left Ventricle	heart
2	chr9:13880600-13899800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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