Variant report

Variant	rs4802965
Chromosome Location	chr19:53015384-53015385
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10582148	0.96[ASN][1000 genomes]
rs11667348	0.94[ASN][1000 genomes]
rs11668903	0.92[ASN][1000 genomes]
rs12462347	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12463002	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12610240	0.96[ASN][1000 genomes]
rs12974840	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12982862	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs162277	0.80[EUR][1000 genomes]
rs162278	0.82[EUR][1000 genomes]
rs172955	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs172956	0.82[JPT][hapmap]
rs2115372	0.87[ASN][1000 genomes]
rs2615587	0.87[CHB][hapmap]
rs2617795	0.83[CHB][hapmap]
rs2633513	0.83[CHB][hapmap]
rs2868688	0.85[ASN][1000 genomes]
rs326441	0.83[CHB][hapmap]
rs326449	0.83[CHB][hapmap]
rs326458	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34222822	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs36039960	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs410046	0.83[CHB][hapmap];0.81[EUR][1000 genomes]
rs413751	0.81[EUR][1000 genomes]
rs414804	0.80[ASN][1000 genomes]
rs422195	0.83[CHB][hapmap]
rs429367	0.83[CHB][hapmap];0.81[EUR][1000 genomes]
rs434709	0.80[EUR][1000 genomes]
rs440545	0.81[EUR][1000 genomes]
rs441549	0.83[CHB][hapmap]
rs441850	0.81[EUR][1000 genomes]
rs445500	0.83[CHB][hapmap];0.81[EUR][1000 genomes]
rs449671	0.81[EUR][1000 genomes]
rs4802964	0.89[ASN][1000 genomes]
rs4802966	0.96[ASN][1000 genomes]
rs4802967	0.96[ASN][1000 genomes]
rs4802970	0.83[JPT][hapmap]
rs490663	0.97[ASN][1000 genomes]
rs521703	0.83[CHB][hapmap]
rs529698	0.83[CHB][hapmap]
rs607477	0.83[CHB][hapmap]
rs62119356	0.86[ASN][1000 genomes]
rs621469	0.82[JPT][hapmap]
rs633763	0.82[JPT][hapmap]
rs650937	0.80[ASN][1000 genomes]
rs656541	0.83[CHB][hapmap]
rs666356	0.82[CHB][hapmap]
rs668882	0.87[CHB][hapmap]
rs685200	0.83[CHB][hapmap]
rs688646	0.81[EUR][1000 genomes]
rs7257823	0.93[ASN][1000 genomes]
rs781129	0.87[CHB][hapmap]
rs8101346	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9676916	0.82[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1066537	chr19:52794424-53044977	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv544060	chr19:52794424-53044977	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv580026	chr19:52937100-53059872	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1063648	chr19:52938131-53041119	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1057296	chr19:52950339-53396986	Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv978841	chr19:52983057-53088237	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	esv3404701	chr19:52986895-53035152	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1058567	chr19:52992455-53021505	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv3440535	chr19:52993529-53035203	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1066717	chr19:52993620-53041995	Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv1064342	chr19:52996710-53041119	ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1055825	chr19:53001299-53037378	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv1055859	chr19:53001299-53041119	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv1060656	chr19:53001299-53041995	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53002600-53021400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr19:53003400-53022600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr19:53003800-53017600	Weak transcription	Fetal Muscle Trunk	muscle
4	chr19:53004600-53015800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr19:53005400-53015800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
6	chr19:53006400-53021200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr19:53006400-53021400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr19:53006600-53015600	Strong transcription	Cortex derived primary cultured neurospheres	brain
9	chr19:53006600-53016200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr19:53006800-53021400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr19:53007000-53021400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr19:53008400-53015600	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr19:53009000-53022600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr19:53011000-53017800	Weak transcription	Right Ventricle	heart
15	chr19:53012200-53016000	ZNF genes & repeats	Adipose Nuclei	Adipose
16	chr19:53012400-53016200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr19:53012600-53015800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr19:53012800-53015600	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr19:53013000-53016000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr19:53013000-53016200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr19:53013000-53016200	Weak transcription	Fetal Stomach	stomach
22	chr19:53013200-53021800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr19:53013400-53016400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr19:53013600-53015600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr19:53013800-53015400	ZNF genes & repeats	Liver	Liver
26	chr19:53013800-53015800	Strong transcription	HUES64 Cell Line	embryonic stem cell
27	chr19:53013800-53018200	Strong transcription	Fetal Muscle Leg	muscle
28	chr19:53014000-53015400	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
29	chr19:53014000-53015400	Strong transcription	Dnd41	blood
30	chr19:53014000-53015600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
31	chr19:53014000-53015600	Strong transcription	Fetal Kidney	kidney
32	chr19:53014000-53015800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr19:53014200-53015600	Strong transcription	Aorta	Aorta
34	chr19:53014200-53016000	Strong transcription	Ovary	ovary
35	chr19:53014400-53015600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr19:53014600-53015400	Strong transcription	Fetal Brain Male	brain
37	chr19:53014800-53015400	Strong transcription	Brain Anterior Caudate	brain
38	chr19:53014800-53015400	ZNF genes & repeats	Psoas Muscle	Psoas
39	chr19:53014800-53015600	ZNF genes & repeats	Brain Angular Gyrus	brain
40	chr19:53014800-53016400	Strong transcription	Brain Germinal Matrix	brain
41	chr19:53014800-53021200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr19:53015000-53015400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
43	chr19:53015000-53015600	Strong transcription	Fetal Lung	lung
44	chr19:53015000-53015600	ZNF genes & repeats	Left Ventricle	heart
45	chr19:53015000-53020600	Strong transcription	Fetal Brain Female	brain
46	chr19:53015200-53015400	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
47	chr19:53015200-53015600	ZNF genes & repeats	HSMMtube	muscle

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