Variant report

Variant	rs1783447
Chromosome Location	chr11:56644173-56644174
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:56640294..56642115-chr11:56642674..56646805,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR5AK2-1	chr11:56643073-56645554	XLOC_009132
2	lnc-OR5AK2-1	chr11:56643073-56644687	ENSG00000255433
3	lnc-OR5AK2-1	chr11:56643073-56645554	ENSG00000255433
4	lnc-OR5AK2-1	chr11:56643073-56645554	NR_110136

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11828859	1.00[JPT][hapmap]
rs12419314	0.97[ASN][1000 genomes]
rs12421316	1.00[JPT][hapmap]
rs1613887	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1632332	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17640885	0.81[ASN][1000 genomes]
rs1783444	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1783445	1.00[ASN][1000 genomes]
rs1783446	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1783450	0.97[ASN][1000 genomes]
rs1783451	1.00[ASN][1000 genomes]
rs1783459	0.83[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs1783465	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1792494	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1792495	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1792496	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1792498	1.00[ASN][1000 genomes]
rs1792499	1.00[ASN][1000 genomes]
rs1792500	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1892787	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1938751	0.97[ASN][1000 genomes]
rs1938759	0.81[ASN][1000 genomes]
rs1938760	0.81[ASN][1000 genomes]
rs2226850	0.97[ASN][1000 genomes]
rs2226851	0.97[ASN][1000 genomes]
rs2374	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4939095	0.97[ASN][1000 genomes]
rs4939097	0.97[ASN][1000 genomes]
rs523098	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs551339	0.83[AFR][1000 genomes]
rs56210588	0.97[ASN][1000 genomes]
rs677946	0.84[AFR][1000 genomes]
rs68039795	0.81[ASN][1000 genomes]
rs684115	0.85[AFR][1000 genomes]
rs7111113	0.82[ASN][1000 genomes]
rs7118645	0.81[ASN][1000 genomes]
rs737368	0.81[ASN][1000 genomes]
rs7930832	0.97[ASN][1000 genomes]
rs7947879	0.81[ASN][1000 genomes]
rs947805	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048328	chr11:56471984-56649908	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	esv2830406	chr11:56481955-56650124	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
3	nsv468577	chr11:56503728-56704042	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
4	nsv555101	chr11:56503728-56704042	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
5	nsv469960	chr11:56605222-56704042	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1045889	chr11:56624365-56737435	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:56642000-56645200	Enhancers	Stomach Mucosa	stomach
2	chr11:56642800-56646000	Weak transcription	Fetal Intestine Small	intestine
3	chr11:56643200-56644400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:56643600-56645000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:56643600-56646000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:56643800-56644600	Enhancers	NHDF-Ad	bronchial
7	chr11:56643800-56644800	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr11:56643800-56644800	Enhancers	Fetal Lung	lung
9	chr11:56643800-56645200	Enhancers	A549	lung
10	chr11:56644000-56644400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:56644000-56644800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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