Variant report

Variant	rs9640043
Chromosome Location	chr7:7583393-7583394
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:7582529..7585016-chr7:7587079..7589582,2	K562	blood:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1013002	0.95[EUR][1000 genomes]
rs1016028	1.00[EUR][1000 genomes]
rs10229961	0.81[EUR][1000 genomes]
rs10276434	0.81[EUR][1000 genomes]
rs11773679	0.81[EUR][1000 genomes]
rs11976831	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11983756	0.86[EUR][1000 genomes]
rs12535954	0.86[EUR][1000 genomes]
rs2051910	0.86[EUR][1000 genomes]
rs2051912	0.86[EUR][1000 genomes]
rs2051913	0.86[EUR][1000 genomes]
rs2051914	0.86[EUR][1000 genomes]
rs2108063	0.81[EUR][1000 genomes]
rs2108064	0.81[EUR][1000 genomes]
rs2108067	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2190248	1.00[EUR][1000 genomes]
rs2348265	0.86[EUR][1000 genomes]
rs2348339	0.95[EUR][1000 genomes]
rs2881888	0.86[EUR][1000 genomes]
rs2881890	0.81[EUR][1000 genomes]
rs3757532	0.83[AFR][1000 genomes]
rs4035104	0.86[EUR][1000 genomes]
rs4380838	0.86[EUR][1000 genomes]
rs4720741	0.95[EUR][1000 genomes]
rs4725005	0.81[EUR][1000 genomes]
rs6463696	0.86[EUR][1000 genomes]
rs6463705	0.86[EUR][1000 genomes]
rs6946022	0.95[EUR][1000 genomes]
rs6946425	0.95[EUR][1000 genomes]
rs6948157	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6948448	0.91[EUR][1000 genomes]
rs6958110	0.81[EUR][1000 genomes]
rs6962939	0.81[EUR][1000 genomes]
rs6964397	1.00[EUR][1000 genomes]
rs6974246	0.86[EUR][1000 genomes]
rs7384200	0.81[EUR][1000 genomes]
rs7783239	0.86[EUR][1000 genomes]
rs7789187	1.00[EUR][1000 genomes]
rs7789287	0.86[EUR][1000 genomes]
rs7791344	0.95[EUR][1000 genomes]
rs7796709	1.00[EUR][1000 genomes]
rs7805565	0.86[EUR][1000 genomes]
rs7806046	0.86[EUR][1000 genomes]
rs7808788	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7810367	0.86[EUR][1000 genomes]
rs9640044	0.86[EUR][1000 genomes]
rs9640045	0.86[EUR][1000 genomes]
rs972600	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949293	chr7:6990891-7711883	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv1019498	chr7:7053923-7668373	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv538721	chr7:7053923-7668373	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv1026758	chr7:7187491-8075259	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
5	nsv887470	chr7:7310023-7655094	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv887472	chr7:7405069-7680697	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
7	nsv606042	chr7:7427535-7876466	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
8	nsv887473	chr7:7497676-7604913	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv1027872	chr7:7516124-7600842	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv1024107	chr7:7516124-7601638	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv887474	chr7:7519603-7679644	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
12	nsv887475	chr7:7519603-7679644	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
13	nsv887476	chr7:7519603-7680697	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
14	nsv887477	chr7:7531819-7810122	Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
15	nsv1032670	chr7:7535515-8017077	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
16	esv3338823	chr7:7581527-7585825	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
17	esv3385574	chr7:7582327-7585025	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
18	esv3422335	chr7:7582452-7585300	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
19	esv3348369	chr7:7582777-7587775	Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
20	esv3375188	chr7:7582802-7584850	Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
21	esv3373826	chr7:7582989-7585159	Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
22	esv3380295	chr7:7583137-7585110	Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
23	esv3343903	chr7:7583164-7585291	Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7575800-7593000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr7:7581800-7595800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:7582600-7588000	Weak transcription	Liver	Liver
4	chr7:7582600-7589600	Weak transcription	Muscle Satellite Cultured Cells	--

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