Variant report

Variant	rs840766
Chromosome Location	chr12:44698441-44698442
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10506245	1.00[ASN][1000 genomes]
rs1098497	1.00[ASN][1000 genomes]
rs1527315	1.00[ASN][1000 genomes]
rs1622682	1.00[ASN][1000 genomes]
rs1625442	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1643432	1.00[ASN][1000 genomes]
rs1643433	1.00[ASN][1000 genomes]
rs1643434	1.00[ASN][1000 genomes]
rs1644007	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1644009	0.80[CEU][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1644010	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1644011	0.83[ASN][1000 genomes]
rs1644014	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1716605	1.00[ASN][1000 genomes]
rs1716606	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1726874	0.83[CEU][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1726879	1.00[ASN][1000 genomes]
rs1726884	1.00[ASN][1000 genomes]
rs1726887	1.00[ASN][1000 genomes]
rs1726888	1.00[ASN][1000 genomes]
rs1726889	1.00[ASN][1000 genomes]
rs1726890	0.83[CEU][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1726900	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1798020	1.00[ASN][1000 genomes]
rs1798023	0.83[CEU][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1798025	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1798026	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1798027	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs58802461	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60441308	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73274199	0.83[ASN][1000 genomes]
rs73276236	1.00[ASN][1000 genomes]
rs73276240	1.00[ASN][1000 genomes]
rs73276275	1.00[ASN][1000 genomes]
rs7958975	1.00[ASN][1000 genomes]
rs840764	1.00[ASN][1000 genomes]
rs840767	1.00[ASN][1000 genomes]
rs840768	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs840772	0.83[ASN][1000 genomes]
rs840773	1.00[ASN][1000 genomes]
rs840774	1.00[ASN][1000 genomes]
rs859016	1.00[ASN][1000 genomes]
rs863482	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1038498	chr12:44679455-44816572	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44682000-44698600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:44688800-44702000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:44690400-44698600	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr12:44690800-44701400	Weak transcription	Left Ventricle	heart
5	chr12:44691400-44701400	Weak transcription	Psoas Muscle	Psoas
6	chr12:44693600-44698600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:44694600-44706000	Weak transcription	Fetal Muscle Trunk	muscle
8	chr12:44695200-44699200	Weak transcription	Brain Anterior Caudate	brain
9	chr12:44697800-44698800	ZNF genes & repeats	HSMMtube	muscle
10	chr12:44697800-44699000	ZNF genes & repeats	Aorta	Aorta
11	chr12:44697800-44699000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
12	chr12:44697800-44699000	ZNF genes & repeats	Fetal Intestine Small	intestine
13	chr12:44697800-44699000	ZNF genes & repeats	Pancreas	Pancrea
14	chr12:44697800-44699000	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
15	chr12:44698000-44698600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr12:44698000-44698800	ZNF genes & repeats	Liver	Liver
17	chr12:44698000-44699000	ZNF genes & repeats	Esophagus	oesophagus
18	chr12:44698200-44699000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr12:44698200-44699000	ZNF genes & repeats	Ovary	ovary
20	chr12:44698200-44700000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr12:44698400-44702800	Weak transcription	Gastric	stomach

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