Variant report

Variant	rs11968077
Chromosome Location	chr6:48718589-48718590
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 119 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs10498777	0.90[ASN][1000 genomes]
rs10807396	0.90[ASN][1000 genomes]
rs11961380	0.85[ASN][1000 genomes]
rs11962463	0.90[ASN][1000 genomes]
rs11963176	0.85[ASN][1000 genomes]
rs11965476	0.85[ASN][1000 genomes]
rs11966759	0.85[ASN][1000 genomes]
rs11967676	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11969013	0.85[ASN][1000 genomes]
rs11969582	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11970453	0.85[ASN][1000 genomes]
rs11970592	0.85[ASN][1000 genomes]
rs12203534	0.85[ASN][1000 genomes]
rs16877973	0.94[AFR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16878182	0.88[ASN][1000 genomes]
rs16878200	0.90[ASN][1000 genomes]
rs16878246	0.85[ASN][1000 genomes]
rs16878250	0.85[ASN][1000 genomes]
rs16878254	0.85[ASN][1000 genomes]
rs16878284	0.85[ASN][1000 genomes]
rs17289986	0.90[ASN][1000 genomes]
rs1938175	0.85[ASN][1000 genomes]
rs1938177	0.85[ASN][1000 genomes]
rs1938178	0.85[ASN][1000 genomes]
rs1938188	0.85[ASN][1000 genomes]
rs1938189	0.85[ASN][1000 genomes]
rs1938200	0.85[ASN][1000 genomes]
rs2154345	0.85[ASN][1000 genomes]
rs2186209	0.85[ASN][1000 genomes]
rs2186210	0.85[ASN][1000 genomes]
rs2396884	0.85[ASN][1000 genomes]
rs2474494	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2495920	0.90[ASN][1000 genomes]
rs34366744	0.85[ASN][1000 genomes]
rs4144036	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4410722	0.80[ASN][1000 genomes]
rs4715097	0.90[ASN][1000 genomes]
rs4715104	0.85[ASN][1000 genomes]
rs55683183	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55843069	0.83[ASN][1000 genomes]
rs56204989	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56975981	0.90[ASN][1000 genomes]
rs57262789	0.91[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57755228	0.85[ASN][1000 genomes]
rs59324209	0.85[ASN][1000 genomes]
rs59704925	0.90[ASN][1000 genomes]
rs60663846	0.85[ASN][1000 genomes]
rs61710291	0.85[ASN][1000 genomes]
rs6458635	0.85[ASN][1000 genomes]
rs6900138	0.90[ASN][1000 genomes]
rs6907951	0.85[ASN][1000 genomes]
rs6907997	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6908335	0.85[ASN][1000 genomes]
rs6914646	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs6927078	0.85[ASN][1000 genomes]
rs6927218	0.85[ASN][1000 genomes]
rs6927449	0.85[ASN][1000 genomes]
rs6927828	0.85[ASN][1000 genomes]
rs6933051	0.85[ASN][1000 genomes]
rs6935064	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs72860717	0.85[ASN][1000 genomes]
rs72860719	0.85[ASN][1000 genomes]
rs72860720	0.85[ASN][1000 genomes]
rs72860732	0.85[ASN][1000 genomes]
rs72860735	0.85[ASN][1000 genomes]
rs72860736	0.80[ASN][1000 genomes]
rs72860742	0.85[ASN][1000 genomes]
rs72860744	0.85[ASN][1000 genomes]
rs72860749	0.85[ASN][1000 genomes]
rs72860750	0.85[ASN][1000 genomes]
rs72860752	0.85[ASN][1000 genomes]
rs72860755	0.85[ASN][1000 genomes]
rs72862035	0.85[ASN][1000 genomes]
rs72862038	0.85[ASN][1000 genomes]
rs72862051	0.85[ASN][1000 genomes]
rs72862062	0.85[ASN][1000 genomes]
rs72862067	0.85[ASN][1000 genomes]
rs72862069	0.85[ASN][1000 genomes]
rs72869027	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72869031	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72869034	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs72869036	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72869052	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72869077	0.94[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72869083	1.00[ASN][1000 genomes]
rs72869092	0.86[AFR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72870818	0.90[ASN][1000 genomes]
rs72870857	0.90[ASN][1000 genomes]
rs72870893	0.90[ASN][1000 genomes]
rs72870898	0.90[ASN][1000 genomes]
rs72870901	0.90[ASN][1000 genomes]
rs72872305	0.90[ASN][1000 genomes]
rs72872308	0.90[ASN][1000 genomes]
rs72872314	0.90[ASN][1000 genomes]
rs72872325	0.88[ASN][1000 genomes]
rs72872343	0.90[ASN][1000 genomes]
rs72872348	0.90[ASN][1000 genomes]
rs72872354	0.90[ASN][1000 genomes]
rs72872357	0.90[ASN][1000 genomes]
rs72872364	0.90[ASN][1000 genomes]
rs72872366	0.90[ASN][1000 genomes]
rs72872368	0.90[ASN][1000 genomes]
rs72872374	0.85[ASN][1000 genomes]
rs72872378	0.85[ASN][1000 genomes]
rs7767482	0.90[ASN][1000 genomes]
rs7770365	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7771117	0.90[ASN][1000 genomes]
rs7774329	0.85[ASN][1000 genomes]
rs9381691	0.90[ASN][1000 genomes]
rs9395402	0.90[ASN][1000 genomes]
rs9395405	0.86[ASN][1000 genomes]
rs9463440	0.90[ASN][1000 genomes]
rs9473472	0.90[ASN][1000 genomes]
rs9473474	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033151	chr6:48067287-48797029	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv538217	chr6:48067287-48797029	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2752125	chr6:48575963-48718589	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv949690	chr6:48595821-49289855	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv885879	chr6:48634956-48730669	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:48715400-48723800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:48717800-48718600	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr6:48718200-48718800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:48718200-48718800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr6:48718200-48718800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr6:48718200-48719400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr6:48718400-48718800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr6:48718400-48719000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr6:48718400-48719000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:48718400-48719200	Enhancers	HUES48 Cell Line	embryonic stem cell

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