Variant report

Variant	rs1365533
Chromosome Location	chr12:74714688-74714689
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1019690	1.00[ASN][1000 genomes]
rs1019692	1.00[ASN][1000 genomes]
rs1019693	1.00[ASN][1000 genomes]
rs1019694	1.00[ASN][1000 genomes]
rs10879749	1.00[ASN][1000 genomes]
rs10879759	0.81[CHB][hapmap];0.88[JPT][hapmap];0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11180015	1.00[ASN][1000 genomes]
rs11180027	0.98[ASN][1000 genomes]
rs11180036	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11180049	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11180057	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs11180063	0.85[ASN][1000 genomes]
rs11608849	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11829422	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs11836857	0.91[ASN][1000 genomes]
rs12422910	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1346248	1.00[ASN][1000 genomes]
rs1365534	1.00[ASN][1000 genomes]
rs1471296	0.85[ASN][1000 genomes]
rs17113126	0.86[JPT][hapmap]
rs17113127	0.88[JPT][hapmap]
rs17113224	0.91[ASN][1000 genomes]
rs17113335	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1820497	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1834669	0.97[ASN][1000 genomes]
rs2012003	1.00[ASN][1000 genomes]
rs2012005	1.00[ASN][1000 genomes]
rs2162395	1.00[ASN][1000 genomes]
rs2169290	0.85[ASN][1000 genomes]
rs2278189	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4883488	0.91[ASN][1000 genomes]
rs4883489	0.91[ASN][1000 genomes]
rs66472931	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs66504708	0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs66512760	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66514235	0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs66661116	0.91[ASN][1000 genomes]
rs66671338	0.81[ASN][1000 genomes]
rs66756307	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs66955885	0.91[ASN][1000 genomes]
rs67027369	0.95[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs67249120	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs67283194	0.92[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs67436776	0.85[ASN][1000 genomes]
rs67452475	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs67619450	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs67630387	0.92[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs67773463	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs68026423	1.00[ASN][1000 genomes]
rs68173977	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72652864	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72652865	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7295476	0.97[ASN][1000 genomes]
rs7299438	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs7305709	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7398187	0.98[ASN][1000 genomes]
rs965780	0.81[ASN][1000 genomes]
rs9788023	0.88[JPT][hapmap]
rs9788180	0.88[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039468	chr12:74080586-75000246	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv899290	chr12:74666737-74729489	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv899291	chr12:74666737-74740958	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1051702	chr12:74674733-74732069	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv428595	chr12:74679884-74858160	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv523765	chr12:74680999-74749476	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv1052996	chr12:74710909-74891621	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv541540	chr12:74710909-74891621	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74711400-74721600	Weak transcription	A549	lung

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