Variant report

Variant	rs704190
Chromosome Location	chr12:22014473-22014474
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10841900	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11046212	0.94[CHB][hapmap];0.85[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11046213	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11046215	0.94[CHB][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1283822	0.82[CEU][hapmap];0.86[AMR][1000 genomes]
rs1643235	0.86[EUR][1000 genomes]
rs1914361	0.83[CHB][hapmap]
rs1972613	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2032775	0.83[CHB][hapmap]
rs2112080	0.82[JPT][hapmap]
rs2161063	0.88[CHB][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2292771	0.84[CHB][hapmap]
rs2307024	0.94[CHB][hapmap];0.83[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3782667	0.82[JPT][hapmap]
rs4148673	0.89[CHB][hapmap];0.83[JPT][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4148674	0.83[CHB][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4296081	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4762717	0.84[CHB][hapmap]
rs704175	0.84[JPT][hapmap]
rs704177	0.86[AMR][1000 genomes]
rs704178	0.85[AMR][1000 genomes]
rs704180	0.80[CEU][hapmap];0.85[AMR][1000 genomes]
rs704182	0.85[AMR][1000 genomes]
rs704185	1.00[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs704187	1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs704189	1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.95[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs704191	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs704192	0.81[CEU][hapmap];0.88[EUR][1000 genomes]
rs7314764	0.84[CHB][hapmap]
rs7966849	0.82[CEU][hapmap];0.90[AMR][1000 genomes]
rs7978092	0.84[CHB][hapmap]
rs829072	0.82[AMR][1000 genomes]
rs829079	0.82[CEU][hapmap];0.86[AMR][1000 genomes]
rs861202	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]

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:17 , 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	chr12:22003400-22015800	Weak transcription	Right Ventricle	heart
8	chr12:22003400-22026600	Weak transcription	Psoas Muscle	Psoas
9	chr12:22003600-22014600	Weak transcription	Adipose Nuclei	Adipose
10	chr12:22003600-22022400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr12:22007800-22022200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr12:22008600-22017800	Strong transcription	Liver	Liver
13	chr12:22009800-22015200	Strong transcription	Skeletal Muscle Female	skeletal muscle
14	chr12:22012200-22026400	Weak transcription	Fetal Heart	heart
15	chr12:22012400-22015200	Weak transcription	Fetal Muscle Trunk	muscle
16	chr12:22014200-22015800	Strong transcription	Left Ventricle	heart
17	chr12:22014200-22020800	Weak transcription	Fetal Lung	lung

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