Variant report

Variant	rs11046212
Chromosome Location	chr12:22006116-22006117
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10841900	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11046213	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11046215	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12825295	0.82[AMR][1000 genomes]
rs1388698	0.86[CHB][hapmap]
rs1643235	1.00[CEU][hapmap];0.81[CHB][hapmap];0.88[JPT][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1914361	0.83[CHB][hapmap]
rs1972613	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2032775	0.83[CHB][hapmap]
rs2098574	0.88[JPT][hapmap]
rs2112080	0.94[JPT][hapmap]
rs2161063	1.00[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2292771	0.84[CHB][hapmap]
rs2307024	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3782667	0.81[CHB][hapmap];0.94[JPT][hapmap]
rs4148666	0.88[CHB][hapmap]
rs4148673	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4148674	0.95[CEU][hapmap];0.87[CHB][hapmap];0.87[JPT][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4296081	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4762717	0.84[CHB][hapmap]
rs704175	0.94[JPT][hapmap]
rs704178	0.81[AMR][1000 genomes]
rs704180	0.81[AMR][1000 genomes]
rs704182	0.81[AMR][1000 genomes]
rs704185	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs704187	0.94[CHB][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs704189	0.94[CHB][hapmap];0.94[JPT][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs704190	0.94[CHB][hapmap];0.85[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs704191	0.88[CHB][hapmap];0.88[JPT][hapmap];0.89[EUR][1000 genomes]
rs704192	0.88[CHB][hapmap];0.88[JPT][hapmap];0.89[EUR][1000 genomes]
rs7314764	0.84[CHB][hapmap]
rs7966849	0.83[AMR][1000 genomes]
rs7978092	0.84[CHB][hapmap]
rs861202	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs864360	0.89[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv557741	chr12:21578559-22169854	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv1051073	chr12:21910875-22271209	Flanking Bivalent TSS/Enh Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv470275	chr12:21938544-22126314	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv1847099	chr12:22003544-22035425	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21973800-22025400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr12:21995600-22022200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr12:21995600-22034800	Weak transcription	Colon Smooth Muscle	Colon
4	chr12:21995800-22022600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr12:21997600-22016600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:21999200-22015400	Weak transcription	Fetal Muscle Leg	muscle
7	chr12:22001400-22011400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr12:22003400-22008600	Weak transcription	Pancreas	Pancrea
9	chr12:22003400-22014200	Weak transcription	Left Ventricle	heart
10	chr12:22003400-22015800	Weak transcription	Right Ventricle	heart
11	chr12:22003400-22026600	Weak transcription	Psoas Muscle	Psoas
12	chr12:22003600-22014600	Weak transcription	Adipose Nuclei	Adipose
13	chr12:22003600-22022400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr12:22004000-22007000	Strong transcription	Liver	Liver
15	chr12:22004000-22010400	Weak transcription	Fetal Heart	heart
16	chr12:22005600-22006600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr12:22005800-22006800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr12:22005800-22007000	Strong transcription	Skeletal Muscle Female	skeletal muscle

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