Variant report

Variant	rs6944926
Chromosome Location	chr7:26842699-26842700
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 136 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:133)

rs_ID	r²[population]
rs10215738	0.90[AFR][1000 genomes]
rs10225924	0.92[AFR][1000 genomes]
rs10227231	0.82[YRI][hapmap];0.82[AFR][1000 genomes]
rs10227529	0.81[AFR][1000 genomes]
rs10227673	0.84[LWK][hapmap];0.83[AFR][1000 genomes]
rs10229837	0.89[AFR][1000 genomes]
rs10236221	0.82[AFR][1000 genomes]
rs10242572	0.81[AFR][1000 genomes]
rs10244986	0.90[AFR][1000 genomes]
rs10248500	0.86[AFR][1000 genomes]
rs10249931	0.86[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10251839	0.82[AFR][1000 genomes]
rs10252275	0.88[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10256250	0.81[AFR][1000 genomes]
rs10259983	0.88[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10262414	0.85[AFR][1000 genomes]
rs10267950	0.93[YRI][hapmap];0.92[AFR][1000 genomes]
rs10270187	0.87[YRI][hapmap];0.82[AFR][1000 genomes]
rs10272190	0.82[YRI][hapmap];0.82[AFR][1000 genomes]
rs10272301	0.84[AFR][1000 genomes]
rs10272303	0.92[AFR][1000 genomes]
rs10272457	0.81[YRI][hapmap];0.82[AFR][1000 genomes]
rs10272603	0.82[AFR][1000 genomes]
rs10275896	0.87[AFR][1000 genomes]
rs10276471	0.93[YRI][hapmap];0.89[AFR][1000 genomes]
rs10280476	0.88[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10281933	1.00[ASW][hapmap];0.84[LWK][hapmap];0.88[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10486483	0.84[LWK][hapmap];0.81[AFR][1000 genomes]
rs10486484	1.00[ASW][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];0.88[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10486485	0.81[AFR][1000 genomes]
rs12333525	0.85[AFR][1000 genomes]
rs12532199	0.89[AFR][1000 genomes]
rs12532395	0.92[AFR][1000 genomes]
rs12534899	0.84[LWK][hapmap];0.83[AFR][1000 genomes]
rs12534921	0.81[AFR][1000 genomes]
rs12535784	0.81[AFR][1000 genomes]
rs12536145	0.81[AFR][1000 genomes]
rs12536560	0.93[YRI][hapmap];0.93[AFR][1000 genomes]
rs12537014	0.83[AFR][1000 genomes]
rs12537323	0.86[AFR][1000 genomes]
rs12540045	0.86[AFR][1000 genomes]
rs12540508	0.83[AFR][1000 genomes]
rs1327988	0.90[LWK][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes]
rs1327989	0.93[YRI][hapmap];0.89[AFR][1000 genomes]
rs13438513	0.89[LWK][hapmap];0.89[AFR][1000 genomes]
rs13438514	0.89[LWK][hapmap];0.85[AFR][1000 genomes]
rs17154529	0.89[ASW][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes]
rs17315334	0.87[AFR][1000 genomes]
rs17315775	0.89[LWK][hapmap];0.89[AFR][1000 genomes]
rs17315929	0.89[LWK][hapmap];0.86[AFR][1000 genomes]
rs17375272	0.80[AFR][1000 genomes]
rs1967332	0.81[AFR][1000 genomes]
rs2030136	0.81[AFR][1000 genomes]
rs2031811	0.81[AFR][1000 genomes]
rs28404962	0.87[AFR][1000 genomes]
rs28550029	0.81[AFR][1000 genomes]
rs28617235	0.85[AFR][1000 genomes]
rs28733208	0.89[AFR][1000 genomes]
rs28806787	0.85[AFR][1000 genomes]
rs28816386	0.82[AFR][1000 genomes]
rs28883078	0.83[AFR][1000 genomes]
rs3213853	0.81[AFR][1000 genomes]
rs3801803	0.89[LWK][hapmap]
rs3801805	0.81[AFR][1000 genomes]
rs3801807	0.89[LWK][hapmap];0.81[AFR][1000 genomes]
rs3801809	0.81[AFR][1000 genomes]
rs3801812	0.82[YRI][hapmap];0.82[AFR][1000 genomes]
rs3801813	0.82[YRI][hapmap];0.82[AFR][1000 genomes]
rs3801814	0.84[AFR][1000 genomes]
rs3801816	0.84[AFR][1000 genomes]
rs3801820	0.89[AFR][1000 genomes]
rs3801821	0.89[AFR][1000 genomes]
rs3801822	0.89[AFR][1000 genomes]
rs3801823	0.83[AFR][1000 genomes]
rs3801825	0.89[AFR][1000 genomes]
rs3801826	0.89[AFR][1000 genomes]
rs3801827	0.89[AFR][1000 genomes]
rs3801828	0.89[AFR][1000 genomes]
rs3801829	0.89[AFR][1000 genomes]
rs3801830	0.88[AFR][1000 genomes]
rs3801831	0.89[AFR][1000 genomes]
rs3801832	0.89[AFR][1000 genomes]
rs3801833	0.89[AFR][1000 genomes]
rs3801834	0.89[AFR][1000 genomes]
rs3801837	0.89[AFR][1000 genomes]
rs3801840	0.93[YRI][hapmap];0.90[AFR][1000 genomes]
rs3801842	0.93[YRI][hapmap];0.89[AFR][1000 genomes]
rs3801843	0.85[LWK][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes]
rs3801844	0.90[LWK][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes]
rs3801848	0.93[YRI][hapmap]
rs3801850	0.93[YRI][hapmap];0.92[AFR][1000 genomes]
rs3823928	0.81[AFR][1000 genomes]
rs3823930	0.89[AFR][1000 genomes]
rs3823931	0.89[AFR][1000 genomes]
rs3823932	0.81[YRI][hapmap];0.89[AFR][1000 genomes]
rs3823933	0.89[AFR][1000 genomes]
rs3823936	0.89[AFR][1000 genomes]
rs3823938	0.89[AFR][1000 genomes]
rs3934268	0.81[AFR][1000 genomes]
rs4722644	0.88[AFR][1000 genomes]
rs4722647	0.81[AFR][1000 genomes]
rs55739485	0.89[AFR][1000 genomes]
rs56154570	0.83[AFR][1000 genomes]
rs57135974	0.89[AFR][1000 genomes]
rs58760954	0.89[AFR][1000 genomes]
rs59254259	0.83[AFR][1000 genomes]
rs61354389	0.83[AFR][1000 genomes]
rs6461980	0.81[AFR][1000 genomes]
rs6948584	0.85[AFR][1000 genomes]
rs6948657	0.89[AFR][1000 genomes]
rs6956088	0.89[AFR][1000 genomes]
rs73065517	0.89[AFR][1000 genomes]
rs73065521	0.89[AFR][1000 genomes]
rs73067435	0.89[AFR][1000 genomes]
rs73067443	0.89[AFR][1000 genomes]
rs73067456	0.88[AFR][1000 genomes]
rs73067475	0.89[AFR][1000 genomes]
rs73067476	0.89[AFR][1000 genomes]
rs73067479	0.86[AFR][1000 genomes]
rs73069507	0.83[AFR][1000 genomes]
rs73069510	0.83[AFR][1000 genomes]
rs7785689	0.86[AFR][1000 genomes]
rs7785711	0.85[AFR][1000 genomes]
rs7785798	0.89[AFR][1000 genomes]
rs7785815	0.89[AFR][1000 genomes]
rs7785832	0.82[YRI][hapmap];0.87[AFR][1000 genomes]
rs7785918	0.87[AFR][1000 genomes]
rs7789225	0.88[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7799888	0.82[LWK][hapmap]
rs7802715	0.84[AFR][1000 genomes]
rs7804356	0.84[LWK][hapmap]
rs7804620	0.81[AFR][1000 genomes]
rs7805766	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
2	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv887855	chr7:26823963-26872652	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	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	chr7:26808000-26854800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:26812400-26849000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr7:26813000-26871200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr7:26821000-26843000	Weak transcription	Fetal Lung	lung
5	chr7:26823000-26846400	Weak transcription	Primary B cells from peripheral blood	blood
6	chr7:26825400-26872400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr7:26836600-26846200	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr7:26837400-26842800	Weak transcription	Primary B cells from cord blood	blood
9	chr7:26839400-26842800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr7:26839400-26871800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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