Variant report

Variant	rs73679950
Chromosome Location	chr7:12363523-12363524
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:12362049..12364322-chr7:12365857..12368217,3	K562	blood:
2	chr7:12359785..12361369-chr7:12363361..12365480,2	K562	blood:
3	chr7:12362078..12365720-chr7:12370304..12373327,3	K562	blood:

Extended variants
information (count: 151 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:137)

rs_ID	r²[population]
rs2192831	0.98[AFR][1000 genomes]
rs2192832	0.98[AFR][1000 genomes]
rs2216047	0.98[AFR][1000 genomes]
rs2356164	0.98[AFR][1000 genomes]
rs2356165	0.98[AFR][1000 genomes]
rs55638440	0.98[AFR][1000 genomes]
rs55664102	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55690557	1.00[AMR][1000 genomes]
rs55717500	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55802346	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55838066	0.98[AFR][1000 genomes]
rs56038003	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56212920	0.98[AFR][1000 genomes]
rs57050876	0.95[AFR][1000 genomes]
rs57429766	0.98[AFR][1000 genomes]
rs57550043	0.98[AFR][1000 genomes]
rs58125710	0.91[AFR][1000 genomes]
rs58430103	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58464800	0.95[AFR][1000 genomes]
rs58848722	0.98[AFR][1000 genomes]
rs59138526	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60783223	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60928801	0.95[AFR][1000 genomes]
rs60964090	1.00[AMR][1000 genomes]
rs61225902	0.86[AFR][1000 genomes]
rs61248493	0.98[AFR][1000 genomes]
rs61275641	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61386156	0.98[AFR][1000 genomes]
rs61394799	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61559614	1.00[AMR][1000 genomes]
rs61600346	0.98[AFR][1000 genomes]
rs61737650	1.00[AMR][1000 genomes]
rs6460922	0.98[AFR][1000 genomes]
rs6460924	0.98[AFR][1000 genomes]
rs6945246	0.98[AFR][1000 genomes]
rs6945314	0.98[AFR][1000 genomes]
rs6945324	0.98[AFR][1000 genomes]
rs6945330	0.98[AFR][1000 genomes]
rs6951687	0.98[AFR][1000 genomes]
rs6951898	0.98[AFR][1000 genomes]
rs6952189	0.98[AFR][1000 genomes]
rs6959148	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6959441	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6959444	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6965649	0.98[AFR][1000 genomes]
rs6969789	0.98[AFR][1000 genomes]
rs6971503	0.98[AFR][1000 genomes]
rs6977409	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6979296	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6979460	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6979661	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73677577	1.00[AMR][1000 genomes]
rs73677581	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73677582	0.83[AFR][1000 genomes]
rs73677583	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73677585	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73677586	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73677587	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73677589	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73677590	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73677594	1.00[AMR][1000 genomes]
rs73677598	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73677602	0.98[AFR][1000 genomes]
rs73678103	1.00[AMR][1000 genomes]
rs73678104	1.00[AMR][1000 genomes]
rs73678106	1.00[AMR][1000 genomes]
rs73678107	1.00[AMR][1000 genomes]
rs73678108	1.00[AMR][1000 genomes]
rs73678110	1.00[AMR][1000 genomes]
rs73678111	1.00[AMR][1000 genomes]
rs73678113	1.00[AMR][1000 genomes]
rs73678115	1.00[AMR][1000 genomes]
rs73678117	1.00[AMR][1000 genomes]
rs73678119	1.00[AMR][1000 genomes]
rs73678120	1.00[AMR][1000 genomes]
rs73678122	1.00[AMR][1000 genomes]
rs73678123	1.00[AMR][1000 genomes]
rs73678126	1.00[AMR][1000 genomes]
rs73679904	0.98[AFR][1000 genomes]
rs73679907	0.98[AFR][1000 genomes]
rs73679909	0.98[AFR][1000 genomes]
rs73679910	0.98[AFR][1000 genomes]
rs73679914	0.98[AFR][1000 genomes]
rs73679917	0.88[AFR][1000 genomes]
rs73679918	1.00[AMR][1000 genomes]
rs73679921	0.93[AFR][1000 genomes]
rs73679922	0.98[AFR][1000 genomes]
rs73679923	0.98[AFR][1000 genomes]
rs73679925	0.98[AFR][1000 genomes]
rs73679929	0.98[AFR][1000 genomes]
rs73679930	0.98[AFR][1000 genomes]
rs73679931	0.98[AFR][1000 genomes]
rs73679932	0.98[AFR][1000 genomes]
rs73679934	0.98[AFR][1000 genomes]
rs73679935	0.98[AFR][1000 genomes]
rs73679938	0.98[AFR][1000 genomes]
rs73679939	0.98[AFR][1000 genomes]
rs73679941	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679943	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679945	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679947	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679948	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679949	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679951	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679952	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679953	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679957	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679959	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679961	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679962	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679963	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679964	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679965	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679966	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679967	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679968	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679969	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679970	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679972	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679973	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73679976	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73680913	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73680919	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73680924	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73680949	1.00[AMR][1000 genomes]
rs73680950	1.00[AMR][1000 genomes]
rs73680951	1.00[AMR][1000 genomes]
rs73680952	1.00[AMR][1000 genomes]
rs73680953	1.00[AMR][1000 genomes]
rs73680954	1.00[AMR][1000 genomes]
rs7779965	0.98[AFR][1000 genomes]
rs7792103	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7798838	0.98[AFR][1000 genomes]
rs7798867	0.98[AFR][1000 genomes]
rs7810598	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7811632	0.98[AFR][1000 genomes]
rs7811810	0.98[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv534432	chr7:12148960-12693032	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv1024554	chr7:12214722-12967418	Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv538735	chr7:12214722-12967418	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	nsv887629	chr7:12304555-12400837	ZNF genes & repeats Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1019021	chr7:12310445-12375516	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv887630	chr7:12323757-12400837	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv1034059	chr7:12342549-12367818	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1029941	chr7:12351595-12444490	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv433030	chr7:12352210-12443042	Enhancers Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv1034475	chr7:12352210-12444490	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv1029098	chr7:12354108-12443042	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv887631	chr7:12360805-12434771	Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv887632	chr7:12360805-12439672	Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12351000-12367600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:12354400-12405000	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:12354800-12364800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:12360400-12367600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr7:12360400-12367800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:12361200-12367800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:12361600-12363600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr7:12361600-12367000	Weak transcription	K562	blood
9	chr7:12362200-12363800	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr7:12362200-12364000	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr7:12363200-12363600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr7:12363200-12364000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr7:12363400-12367600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr7:12363400-12367800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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