Variant report

Variant	rs10784028
Chromosome Location	chr12:60539203-60539204
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 111 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10506408	0.87[EUR][1000 genomes]
rs10784027	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10784029	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10784033	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10877392	0.83[EUR][1000 genomes]
rs10877398	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10877399	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10877401	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10877402	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10877403	0.82[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10877406	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11173319	0.87[AMR][1000 genomes]
rs11173327	0.84[EUR][1000 genomes]
rs11173328	0.86[EUR][1000 genomes]
rs11173329	0.86[EUR][1000 genomes]
rs11173336	0.86[EUR][1000 genomes]
rs11173338	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11173339	0.87[EUR][1000 genomes]
rs11173340	0.85[EUR][1000 genomes]
rs11173341	0.87[EUR][1000 genomes]
rs11173343	0.87[EUR][1000 genomes]
rs11173345	0.84[EUR][1000 genomes]
rs11173346	0.84[EUR][1000 genomes]
rs11173357	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11173365	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11173371	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11173387	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12230817	0.81[EUR][1000 genomes]
rs12231312	0.84[EUR][1000 genomes]
rs12817959	0.84[AMR][1000 genomes]
rs12830074	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1304313	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1354469	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1389255	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1389256	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1493311	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1493318	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1493325	0.83[EUR][1000 genomes]
rs1504444	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1587821	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs17595010	0.87[EUR][1000 genomes]
rs17595325	0.91[CEU][hapmap];0.81[CHB][hapmap];0.87[EUR][1000 genomes]
rs17595367	0.87[EUR][1000 genomes]
rs17665306	0.91[CEU][hapmap];0.81[CHB][hapmap];0.86[EUR][1000 genomes]
rs1910674	0.84[AMR][1000 genomes]
rs2014074	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2134882	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2172500	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35713358	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3847662	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3847663	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3907482	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4093759	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4254103	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4347425	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4366523	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4406858	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4454757	0.83[EUR][1000 genomes]
rs4491264	0.84[EUR][1000 genomes]
rs4567505	0.84[EUR][1000 genomes]
rs4625509	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4758743	0.84[EUR][1000 genomes]
rs4758744	0.82[EUR][1000 genomes]
rs4758745	0.82[EUR][1000 genomes]
rs4758855	0.92[AMR][1000 genomes]
rs4758858	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61127975	0.80[EUR][1000 genomes]
rs61922949	0.80[EUR][1000 genomes]
rs61922950	0.80[EUR][1000 genomes]
rs61923065	0.87[EUR][1000 genomes]
rs61923066	0.90[EUR][1000 genomes]
rs61923067	0.83[EUR][1000 genomes]
rs61925366	0.84[EUR][1000 genomes]
rs66587505	0.86[EUR][1000 genomes]
rs7134663	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7135031	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7136435	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7138854	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72648145	0.87[EUR][1000 genomes]
rs7297548	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7298315	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7300532	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7302607	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7310323	0.82[EUR][1000 genomes]
rs7313364	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7314355	0.82[EUR][1000 genomes]
rs735926	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7961221	0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7961816	0.85[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7967860	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7973156	0.85[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7973882	0.83[EUR][1000 genomes]
rs7977065	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7977642	0.80[EUR][1000 genomes]
rs7979069	0.82[EUR][1000 genomes]
rs8181648	0.91[CEU][hapmap];0.81[CHB][hapmap];0.80[EUR][1000 genomes]
rs958543	0.88[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9668893	0.82[EUR][1000 genomes]
rs992478	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428591	chr12:60446360-60631044	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv427913	chr12:60462443-60569344	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	esv2760273	chr12:60489188-60561925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv511495	chr12:60518599-60541932	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv559107	chr12:60518842-60540108	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv559108	chr12:60518842-60548334	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv559119	chr12:60522630-60540108	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv1793962	chr12:60522630-60541932	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv1846332	chr12:60522725-60541932	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv1851665	chr12:60522725-60549171	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv559129	chr12:60522829-60540108	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv559136	chr12:60523425-60540108	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60536800-60540600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr12:60537000-60540000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:60538800-60540000	Weak transcription	K562	blood

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