Variant report

Variant	rs7802934
Chromosome Location	chr7:87672045-87672046
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10235694	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10241669	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10266440	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10279744	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10279940	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10282572	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10435251	0.87[AFR][1000 genomes]
rs10952906	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11770982	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11972409	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12669586	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12704375	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12704380	0.88[EUR][1000 genomes]
rs12704381	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1613737	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1623535	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1629569	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1631368	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1637487	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1637488	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1637489	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1637496	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1637497	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1637498	0.87[EUR][1000 genomes]
rs1637499	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1637502	0.84[EUR][1000 genomes]
rs1637503	0.85[EUR][1000 genomes]
rs1637504	0.84[EUR][1000 genomes]
rs1637505	0.81[EUR][1000 genomes]
rs1637506	0.83[EUR][1000 genomes]
rs1637508	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1688886	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1688887	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1688888	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1688890	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1688891	0.87[EUR][1000 genomes]
rs1688893	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1688894	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1688895	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1688896	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1688897	0.88[EUR][1000 genomes]
rs1688898	0.89[EUR][1000 genomes]
rs1688899	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1688901	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17150161	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2021741	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2022160	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2022163	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2022164	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2023533	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2024018	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2024019	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2079422	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2079423	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2097917	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2158766	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2282948	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2282949	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2282951	0.87[AFR][1000 genomes]
rs2373486	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2373487	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28432284	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28794871	0.83[EUR][1000 genomes]
rs4728718	0.85[EUR][1000 genomes]
rs56050913	0.87[AFR][1000 genomes]
rs56160917	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56897831	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58850563	0.87[AFR][1000 genomes]
rs59135798	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60069756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62486383	0.87[AFR][1000 genomes]
rs6465124	0.82[EUR][1000 genomes]
rs6465127	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7786538	0.82[EUR][1000 genomes]
rs7803521	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9641021	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888677	chr7:86802025-87781111	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1015862	chr7:87075394-88049798	Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1023352	chr7:87418818-88192925	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv539005	chr7:87418818-88192925	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
5	nsv525073	chr7:87535096-87812968	Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1021303	chr7:87646755-87672380	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv607731	chr7:87666666-87672308	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv437021	chr7:87666666-87674671	Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv15186	chr7:87668826-87672870	Flanking Active TSS Weak transcription Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv607735	chr7:87669005-87672308	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv607736	chr7:87669005-87672426	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv607737	chr7:87669005-87672670	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv2421625	chr7:87670739-87672392	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv442056	chr7:87670739-87672392	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	esv2764029	chr7:87670741-87672392	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv514430	chr7:87670784-87672216	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:87670600-87675000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr7:87671400-87672200	Enhancers	Brain Hippocampus Middle	brain
3	chr7:87671400-87674800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:87671600-87672200	Enhancers	Adipose Nuclei	Adipose
5	chr7:87671600-87672200	Enhancers	Brain Anterior Caudate	brain
6	chr7:87671800-87675000	Weak transcription	Brain Angular Gyrus	brain
7	chr7:87672000-87672200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:87672000-87672200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:87672000-87672200	Flanking Active TSS	GM12878-XiMat	blood
10	chr7:87672000-87674800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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