Variant report

Variant	rs8110814
Chromosome Location	chr19:21704845-21704846
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 33 )

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs1012040	0.88[YRI][hapmap]
rs10406824	0.94[YRI][hapmap]
rs1055753	0.95[JPT][hapmap]
rs11085447	0.85[CHD][hapmap];0.95[JPT][hapmap]
rs11085456	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11666680	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11667770	0.94[JPT][hapmap]
rs11668682	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12461802	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12609768	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12610154	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12973084	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12974329	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12975081	0.95[JPT][hapmap]
rs12975424	0.83[EUR][1000 genomes]
rs12981564	0.95[JPT][hapmap]
rs12981735	0.89[JPT][hapmap]
rs12982282	0.95[JPT][hapmap]
rs12985995	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1401926	0.96[CEU][hapmap];0.89[CHB][hapmap];0.93[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.95[TSI][hapmap];0.81[ASN][1000 genomes]
rs1607664	0.94[YRI][hapmap]
rs1813234	0.83[CHB][hapmap];0.88[CHD][hapmap];0.82[JPT][hapmap]
rs1879237	0.81[ASN][1000 genomes]
rs1879238	0.80[ASN][1000 genomes]
rs1984771	0.94[YRI][hapmap]
rs2012013	0.82[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap]
rs2088762	0.87[CHD][hapmap];0.95[JPT][hapmap]
rs2133820	0.94[YRI][hapmap]
rs2133822	0.96[CEU][hapmap];0.88[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2170024	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs2173724	0.80[YRI][hapmap]
rs2246914	0.83[YRI][hapmap]
rs2358984	0.88[CHB][hapmap]
rs2562399	0.94[YRI][hapmap]
rs2562448	0.93[YRI][hapmap]
rs2650791	0.85[YRI][hapmap]
rs2650793	0.82[JPT][hapmap]
rs2650805	0.82[JPT][hapmap]
rs2650845	0.82[CHB][hapmap];0.86[CHD][hapmap]
rs2681371	0.82[YRI][hapmap]
rs28898308	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2914638	0.82[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap]
rs34040704	0.81[ASN][1000 genomes]
rs34497957	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35782355	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4315457	0.88[CHD][hapmap];0.95[JPT][hapmap]
rs4341872	0.83[CHB][hapmap]
rs4462731	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4621113	0.90[JPT][hapmap]
rs56346453	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6511239	0.95[JPT][hapmap]
rs6511253	0.82[JPT][hapmap]
rs6511255	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6511259	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7247411	0.88[CHD][hapmap];0.95[JPT][hapmap]
rs7248601	0.89[JPT][hapmap]
rs7249412	0.95[JPT][hapmap]
rs7249636	0.83[CHB][hapmap];0.88[CHD][hapmap];0.82[JPT][hapmap]
rs7250360	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7250838	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7251540	0.82[EUR][1000 genomes]
rs7251620	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7252254	0.96[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7252261	0.88[CHD][hapmap];0.95[JPT][hapmap]
rs7253249	1.00[CEU][hapmap];0.88[CHB][hapmap];0.84[JPT][hapmap]
rs7253559	0.81[ASN][1000 genomes]
rs7256389	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7257186	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7257857	0.88[CHD][hapmap];0.84[GIH][hapmap];0.95[JPT][hapmap]
rs7259311	0.95[JPT][hapmap]
rs7259317	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73017722	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7508671	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs8099940	0.95[JPT][hapmap]
rs8100318	0.94[YRI][hapmap]
rs8101089	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8101900	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8103325	0.88[CHD][hapmap];0.95[JPT][hapmap]
rs8103459	0.94[JPT][hapmap];0.82[YRI][hapmap]
rs8106840	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8109536	0.80[ASN][1000 genomes]
rs8109940	1.00[CEU][hapmap];0.89[CHB][hapmap];0.90[JPT][hapmap]
rs8110967	0.95[JPT][hapmap]
rs8111885	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs924487	0.84[CHB][hapmap];0.91[JPT][hapmap]
rs9789284	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3518033	chr19:21278465-21747567	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3518034	chr19:21278465-21747567	ZNF genes & repeats Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	esv3414204	chr19:21301761-21839451	ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv3325271	chr19:21445407-21792817	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	esv2751783	chr19:21465822-21726337	Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	esv3363678	chr19:21483148-21756908	Strong transcription Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv578952	chr19:21535707-21868584	Genic enhancers Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	nsv833782	chr19:21663537-21845722	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
9	nsv510759	chr19:21664791-21723191	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	esv2762028	chr19:21685778-21755476	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv963024	chr19:21686690-21722618	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1059328	chr19:21691123-21775948	Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:33)

SNP	Gene	Cis/trans	Tissue	Source
rs8110814	RP11-678G14.2	cis	Muscle Skeletal	GTEx
rs8110814	ZNF429	cis	multi-tissue	Pritchard
rs8110814	CTD-2561J22.5	cis	Skin Sun Exposed Lower leg	GTEx
rs8110814	CTD-2561J22.5	cis	Esophagus Muscularis	GTEx
rs8110814	RP11-678G14.2	cis	Nerve Tibial	GTEx
rs8110814	RP11-678G14.3	cis	lung	GTEx
rs8110814	ZNF429	cis	Whole Blood	GTEx
rs8110814	CTD-2561J22.5	cis	Nerve Tibial	GTEx
rs8110814	RP11-678G14.2	cis	Adipose Subcutaneous	GTEx
rs8110814	CTD-2561J22.5	cis	Thyroid	GTEx
rs8110814	CTD-2561J22.5	cis	Artery Tibial	GTEx
rs8110814	CTD-2561J22.5	cis	lung	GTEx
rs8110814	RP11-678G14.3	cis	Muscle Skeletal	GTEx
rs8110814	RP11-678G14.2	cis	Thyroid	GTEx
rs8110814	RP11-678G14.2	cis	Artery Tibial	GTEx
rs8110814	RP11-678G14.2	cis	lung	GTEx
rs8110814	ZNF708	cis	Skin Sun Exposed Lower leg	GTEx
rs8110814	RP11-420K14.2	cis	Whole Blood	GTEx
rs8110814	RP11-420K14.2	cis	Heart Left Ventricle	GTEx
rs8110814	ZNF738	Cis_1M	lymphoblastoid	RTeQTL
rs8110814	ZNF493	cis	Lymphoblastoid	GTEx
rs8110814	RP11-420K14.1	cis	Muscle Skeletal	GTEx
rs8110814	ZNF493	Cis_1M	lymphoblastoid	RTeQTL
rs8110814	RP11-678G14.3	cis	Whole Blood	GTEx
rs8110814	RP11-678G14.3	cis	Adipose Subcutaneous	GTEx
rs8110814	ZNF100	cis	Muscle Skeletal	GTEx
rs8110814	RP11-678G14.2	cis	Whole Blood	GTEx
rs8110814	RP11-678G14.2	cis	Skin Sun Exposed Lower leg	GTEx
rs8110814	RP11-678G14.3	cis	Skin Sun Exposed Lower leg	GTEx
rs8110814	CTD-2626G11.2	cis	Skin Sun Exposed Lower leg	GTEx
rs8110814	ZNF429	cis	Muscle Skeletal	GTEx
rs8110814	ZNF493	cis	multi-tissue	Pritchard
rs8110814	CTD-2561J22.5	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21698400-21710800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr19:21699400-21705400	ZNF genes & repeats	Dnd41	blood
3	chr19:21699600-21707600	ZNF genes & repeats	Brain Germinal Matrix	brain
4	chr19:21699600-21720800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
5	chr19:21699600-21727600	ZNF genes & repeats	Liver	Liver
6	chr19:21700600-21707800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
7	chr19:21700600-21707800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr19:21700800-21705400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
9	chr19:21700800-21706600	ZNF genes & repeats	Primary B cells from cord blood	blood
10	chr19:21700800-21706800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
11	chr19:21700800-21707200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
12	chr19:21700800-21711000	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
13	chr19:21701000-21705200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
14	chr19:21701000-21706200	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
15	chr19:21701000-21707000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr19:21701000-21707800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr19:21701000-21733400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr19:21701400-21705000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr19:21701400-21707000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
20	chr19:21701400-21707200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
21	chr19:21701400-21707600	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
22	chr19:21701400-21707600	ZNF genes & repeats	Fetal Brain Female	brain
23	chr19:21701400-21708000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
24	chr19:21701600-21705000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr19:21701600-21705000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
26	chr19:21701600-21705400	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr19:21701600-21706200	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
28	chr19:21701600-21706400	Strong transcription	Placenta Amnion	Placenta Amnion
29	chr19:21701600-21706800	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
30	chr19:21701600-21707200	ZNF genes & repeats	Adipose Nuclei	Adipose
31	chr19:21701600-21707200	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
32	chr19:21701600-21712600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr19:21701600-21720400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
34	chr19:21702400-21721400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr19:21702600-21706200	Weak transcription	NH-A	brain
36	chr19:21702600-21713400	Weak transcription	Right Ventricle	heart
37	chr19:21702600-21713400	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr19:21702600-21717200	Weak transcription	Psoas Muscle	Psoas
39	chr19:21702800-21707200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr19:21702800-21713400	Weak transcription	Brain Angular Gyrus	brain
41	chr19:21702800-21717200	Weak transcription	Brain Cingulate Gyrus	brain
42	chr19:21702800-21718600	Weak transcription	Colon Smooth Muscle	Colon
43	chr19:21702800-21718600	Weak transcription	Fetal Heart	heart
44	chr19:21703000-21705000	Strong transcription	HSMM	muscle
45	chr19:21703000-21706400	Weak transcription	Fetal Brain Male	brain
46	chr19:21703000-21706600	Strong transcription	Placenta	Placenta
47	chr19:21703000-21706600	Weak transcription	Stomach Mucosa	stomach
48	chr19:21703000-21707000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr19:21703000-21713400	Weak transcription	Brain Anterior Caudate	brain
50	chr19:21703600-21706400	Strong transcription	Osteobl	bone

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