Variant report

Variant	rs7966732
Chromosome Location	chr12:41790191-41790192
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs1026462	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs1026464	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs10506191	0.91[CHB][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes]
rs10506192	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs10785235	0.81[CHB][hapmap];0.95[JPT][hapmap]
rs10785258	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10785259	0.98[ASN][1000 genomes]
rs10785261	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.99[ASN][1000 genomes]
rs10785265	0.86[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap]
rs10880063	0.91[CHB][hapmap];0.84[CHD][hapmap];0.91[JPT][hapmap];0.92[MEX][hapmap];0.88[ASN][1000 genomes]
rs10880067	0.91[CHB][hapmap];0.86[CHD][hapmap];0.91[JPT][hapmap];0.92[MEX][hapmap]
rs10880071	0.80[MEX][hapmap]
rs11180834	0.81[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs11180836	0.90[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs11180843	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11180851	0.83[CHB][hapmap];0.86[CHD][hapmap];0.91[JPT][hapmap];0.92[MEX][hapmap];0.88[ASN][1000 genomes]
rs11180863	0.91[CHB][hapmap];0.86[CHD][hapmap];0.91[JPT][hapmap];0.92[MEX][hapmap]
rs11180864	0.91[CHB][hapmap];0.86[CHD][hapmap];0.91[JPT][hapmap];0.92[MEX][hapmap]
rs11835941	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12146801	0.87[ASN][1000 genomes]
rs12369680	0.90[CHB][hapmap];0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs12422274	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12578784	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12817575	0.91[CHB][hapmap];0.86[CHD][hapmap];0.91[JPT][hapmap];0.92[MEX][hapmap];0.87[ASN][1000 genomes]
rs1379768	0.86[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap]
rs1379769	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs1405552	1.00[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1458156	0.86[CHB][hapmap];0.81[CHD][hapmap];0.91[JPT][hapmap]
rs1458157	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs1471161	0.86[CHB][hapmap];0.91[CHD][hapmap];0.91[JPT][hapmap]
rs1527090	0.86[CHB][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs1534279	0.83[ASN][1000 genomes]
rs1544000	0.88[ASN][1000 genomes]
rs1902907	1.00[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1902909	0.98[ASN][1000 genomes]
rs1902911	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1918226	0.88[ASN][1000 genomes]
rs2405911	0.88[ASN][1000 genomes]
rs2468315	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs2608711	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs2730803	0.86[CHB][hapmap];0.82[CHD][hapmap];0.91[JPT][hapmap]
rs2730814	0.82[CHB][hapmap];0.82[CHD][hapmap];0.91[JPT][hapmap]
rs2730827	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs2730830	0.86[CHB][hapmap];0.91[CHD][hapmap];0.91[JPT][hapmap]
rs2733269	0.82[CHB][hapmap];0.84[CHD][hapmap];0.91[JPT][hapmap]
rs2733289	0.86[CHB][hapmap];0.90[JPT][hapmap]
rs2897268	0.91[CHB][hapmap];0.86[CHD][hapmap];0.91[JPT][hapmap];0.92[MEX][hapmap];0.88[ASN][1000 genomes]
rs34220247	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6582334	0.88[ASN][1000 genomes]
rs6582336	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7301366	0.99[ASN][1000 genomes]
rs7315276	0.99[ASN][1000 genomes]
rs7956320	0.90[CHB][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs7960955	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7963312	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs7967532	0.97[ASN][1000 genomes]
rs7979586	0.88[ASN][1000 genomes]
rs930905	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs961337	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9783512	0.98[ASN][1000 genomes]
rs981014	0.86[CHB][hapmap];0.91[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832383	chr12:41693298-41846934	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
2	nsv832384	chr12:41772648-41971430	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv899036	chr12:41777144-41807859	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
4	nsv899037	chr12:41777144-41819215	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv1044910	chr12:41778831-41813198	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
6	esv2761735	chr12:41780758-41811938	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
7	esv2757501	chr12:41780758-41816002	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
8	esv2759896	chr12:41780758-41816002	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
9	esv2755020	chr12:41780758-41820936	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
10	nsv899038	chr12:41784137-41819215	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
11	nsv818915	chr12:41784997-41811063	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
12	nsv899039	chr12:41784997-41813207	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a
13	nsv1050627	chr12:41789891-41809009	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7966732	PDZRN4	cis	parietal	SCAN

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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