Variant report

Variant	rs60447835
Chromosome Location	chr14:41046266-41046267
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs11845273	1.00[ASN][1000 genomes]
rs11845336	1.00[ASN][1000 genomes]
rs11848750	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11849724	1.00[ASN][1000 genomes]
rs11850528	1.00[ASN][1000 genomes]
rs12146972	1.00[ASN][1000 genomes]
rs12147443	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12147451	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12147463	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12147713	1.00[ASN][1000 genomes]
rs12147822	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12883741	1.00[ASN][1000 genomes]
rs12886308	1.00[ASN][1000 genomes]
rs12887970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12889214	1.00[ASN][1000 genomes]
rs12896157	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1888590	0.92[ASN][1000 genomes]
rs1958879	0.92[ASN][1000 genomes]
rs1958882	0.92[ASN][1000 genomes]
rs1958883	0.92[ASN][1000 genomes]
rs1959248	0.92[ASN][1000 genomes]
rs2050485	0.90[ASN][1000 genomes]
rs2050486	0.90[ASN][1000 genomes]
rs2415621	1.00[ASN][1000 genomes]
rs2783773	0.92[ASN][1000 genomes]
rs2783774	0.90[ASN][1000 genomes]
rs2899913	1.00[ASN][1000 genomes]
rs2899914	1.00[ASN][1000 genomes]
rs2899915	1.00[ASN][1000 genomes]
rs34074136	0.87[ASN][1000 genomes]
rs34895240	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34984881	1.00[ASN][1000 genomes]
rs35263612	1.00[ASN][1000 genomes]
rs35879367	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35890094	1.00[ASN][1000 genomes]
rs4318119	0.99[ASN][1000 genomes]
rs4347536	0.99[ASN][1000 genomes]
rs4347537	1.00[ASN][1000 genomes]
rs4351965	0.98[ASN][1000 genomes]
rs4414393	1.00[ASN][1000 genomes]
rs4414394	1.00[ASN][1000 genomes]
rs4539502	0.98[ASN][1000 genomes]
rs55830630	1.00[ASN][1000 genomes]
rs56117887	1.00[ASN][1000 genomes]
rs56313047	1.00[ASN][1000 genomes]
rs57195280	1.00[ASN][1000 genomes]
rs60023161	1.00[ASN][1000 genomes]
rs66723010	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7146536	0.92[ASN][1000 genomes]
rs72676201	1.00[ASN][1000 genomes]
rs72679007	0.98[ASN][1000 genomes]
rs72679008	0.99[ASN][1000 genomes]
rs72679011	1.00[ASN][1000 genomes]
rs9323027	0.89[ASN][1000 genomes]
rs9323028	0.89[ASN][1000 genomes]
rs9783594	0.99[ASN][1000 genomes]
rs9783624	1.00[ASN][1000 genomes]
rs9783657	1.00[ASN][1000 genomes]
rs9783668	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv901664	chr14:40663978-41432350	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv901669	chr14:40832004-41432350	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv901675	chr14:40907992-41060034	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv901677	chr14:40912447-41053909	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv901679	chr14:40913662-41053909	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv564463	chr14:40931087-41207433	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv1054806	chr14:40936163-41211004	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv1045757	chr14:40956143-41190589	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv1041122	chr14:40956143-41869421	Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv832777	chr14:40957165-41154628	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv564464	chr14:40957542-41871875	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv1044695	chr14:40959813-41234793	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	nsv542051	chr14:40959813-41234793	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	nsv534448	chr14:40960013-41634431	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
15	nsv994955	chr14:41018728-41234652	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
16	nsv901680	chr14:41023693-41115280	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv1040945	chr14:41043918-41161543	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
18	esv2760338	chr14:41043930-41173768	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:41045800-41046400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:41046000-41046400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr14:41046000-41046400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr14:41046200-41046400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr14:41046200-41046600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:41046200-41046600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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