Variant report

Variant	rs704182
Chromosome Location	chr12:22002568-22002569
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10841900	0.81[AMR][1000 genomes]
rs11046212	0.81[AMR][1000 genomes]
rs11046213	0.81[AMR][1000 genomes]
rs11046215	0.81[AMR][1000 genomes]
rs1283816	0.90[CHB][hapmap];0.81[AMR][1000 genomes]
rs1283817	0.90[CHB][hapmap];0.83[AMR][1000 genomes]
rs1283822	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1299731	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1643235	0.88[AMR][1000 genomes]
rs1967534	0.95[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1972613	0.85[AMR][1000 genomes]
rs2161063	0.81[AMR][1000 genomes]
rs2307024	0.83[AMR][1000 genomes]
rs4148673	0.81[AMR][1000 genomes]
rs4296081	0.87[AMR][1000 genomes]
rs704176	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs704177	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs704178	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs704180	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs704185	0.89[AMR][1000 genomes]
rs704187	0.82[CEU][hapmap];0.87[AMR][1000 genomes]
rs704189	0.82[CEU][hapmap];0.89[AMR][1000 genomes]
rs704190	0.85[AMR][1000 genomes]
rs7966849	1.00[CEU][hapmap];0.86[CHB][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs829068	0.91[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes]
rs829069	0.95[CHB][hapmap];0.86[JPT][hapmap];0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs829072	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs829079	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs829080	1.00[CHB][hapmap];0.84[JPT][hapmap];0.94[YRI][hapmap];0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs861202	0.86[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21958400-22003000	Weak transcription	Psoas Muscle	Psoas
2	chr12:21973800-22025400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:21980600-22002800	Weak transcription	Fetal Heart	heart
4	chr12:21983600-22002800	Strong transcription	Liver	Liver
5	chr12:21983800-22003000	Weak transcription	Pancreas	Pancrea
6	chr12:21985000-22003000	Weak transcription	Right Ventricle	heart
7	chr12:21985400-22005000	Weak transcription	NHLF	lung
8	chr12:21985600-22002800	Weak transcription	Fetal Lung	lung
9	chr12:21985800-22004800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr12:21995400-22003200	Weak transcription	Adipose Nuclei	Adipose
11	chr12:21995600-22004400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr12:21995600-22022200	Weak transcription	Stomach Smooth Muscle	stomach
13	chr12:21995600-22034800	Weak transcription	Colon Smooth Muscle	Colon
14	chr12:21995800-22022600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr12:21997600-22016600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:21998400-22003000	Weak transcription	Left Ventricle	heart
17	chr12:21999200-22015400	Weak transcription	Fetal Muscle Leg	muscle
18	chr12:21999800-22003600	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr12:22001400-22011400	Weak transcription	Fetal Muscle Trunk	muscle
20	chr12:22001600-22002800	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr12:22002000-22003000	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr12:22002000-22003200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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