Variant report

Variant	rs560389
Chromosome Location	chr1:92647223-92647224
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:91965368..91967670-chr1:92645246..92647453,2	K562	blood:

Variant related genes	Relation type
ENSG00000097046	Chromatin interaction

Extended variants
information (count: 108 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10159094	0.91[CEU][hapmap]
rs10747503	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10875204	0.80[CEU][hapmap]
rs10875209	0.84[CEU][hapmap];1.00[JPT][hapmap]
rs10875214	0.87[CEU][hapmap]
rs10875237	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1157469	0.88[CEU][hapmap];0.82[TSI][hapmap]
rs1157470	0.87[CEU][hapmap]
rs11577572	1.00[ASW][hapmap];0.87[CEU][hapmap];0.84[GIH][hapmap];0.87[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs11585255	1.00[YRI][hapmap]
rs11588044	1.00[ASW][hapmap];0.87[CEU][hapmap];0.81[GIH][hapmap];0.87[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs11588153	1.00[ASW][hapmap];0.87[CEU][hapmap];0.81[GIH][hapmap];0.91[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs11589858	0.87[CEU][hapmap];0.81[GIH][hapmap];0.95[TSI][hapmap]
rs12119246	0.84[CEU][hapmap]
rs1226176	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1226179	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1226183	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1226187	0.88[CEU][hapmap];0.89[ASN][1000 genomes]
rs12404806	0.86[CEU][hapmap];1.00[YRI][hapmap]
rs12724638	0.86[CEU][hapmap];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12729867	0.91[CEU][hapmap];0.90[GIH][hapmap];0.95[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap]
rs12734478	0.87[CEU][hapmap];0.90[GIH][hapmap];0.95[MEX][hapmap];0.88[MKK][hapmap];0.95[TSI][hapmap]
rs12740246	0.87[CEU][hapmap]
rs12753920	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12755781	1.00[ASW][hapmap];0.87[CEU][hapmap];0.81[GIH][hapmap];0.87[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs12757533	0.87[CEU][hapmap]
rs12759512	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1384612	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1384613	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1466514	0.82[EUR][1000 genomes]
rs1483022	0.91[CEU][hapmap];0.90[TSI][hapmap];0.90[ASN][1000 genomes]
rs17519385	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17578686	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1982720	0.88[CEU][hapmap]
rs2069051	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2093879	0.84[CEU][hapmap]
rs2181897	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2391114	0.91[CEU][hapmap]
rs2839877	0.88[CEU][hapmap]
rs2893200	0.88[CEU][hapmap];0.82[TSI][hapmap]
rs3103181	1.00[JPT][hapmap]
rs3118137	0.90[ASN][1000 genomes]
rs35015161	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3851271	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs3851272	0.88[CEU][hapmap];0.82[TSI][hapmap]
rs3851273	0.87[CEU][hapmap]
rs4437922	0.84[CEU][hapmap]
rs4658128	0.84[CEU][hapmap]
rs4658290	0.83[CEU][hapmap]
rs4658294	0.91[CEU][hapmap];0.90[GIH][hapmap];0.95[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4658298	0.86[CEU][hapmap];1.00[YRI][hapmap]
rs4658299	1.00[ASW][hapmap];0.87[CEU][hapmap];0.84[GIH][hapmap];0.87[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs488288	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs488849	0.88[CEU][hapmap];0.89[ASN][1000 genomes]
rs490800	0.91[CEU][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs492164	0.96[CEU][hapmap];0.87[GIH][hapmap];0.84[TSI][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs493595	0.91[CEU][hapmap];0.89[ASN][1000 genomes]
rs4949888	1.00[ASW][hapmap];0.87[CEU][hapmap];0.81[GIH][hapmap];0.81[LWK][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap]
rs504606	0.83[CEU][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs504613	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs504706	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs506375	1.00[ASW][hapmap];0.96[CEU][hapmap];0.90[GIH][hapmap];0.95[MKK][hapmap];0.85[TSI][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs506377	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs507452	0.89[ASN][1000 genomes]
rs511546	0.91[CEU][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs515280	1.00[CEU][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs519343	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs519623	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs519932	1.00[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs527412	0.91[CEU][hapmap];0.87[GIH][hapmap];0.89[ASN][1000 genomes]
rs529135	0.89[ASN][1000 genomes]
rs534547	0.83[CEU][hapmap];0.89[ASN][1000 genomes]
rs539288	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs544557	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs547699	0.91[CEU][hapmap];0.89[ASN][1000 genomes]
rs551909	0.95[CEU][hapmap];0.89[ASN][1000 genomes]
rs553861	0.91[CEU][hapmap];0.89[ASN][1000 genomes]
rs556980	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs563113	0.96[CEU][hapmap];0.90[GIH][hapmap];0.85[TSI][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs563606	0.81[GIH][hapmap];0.89[ASN][1000 genomes]
rs564971	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs569178	0.89[ASN][1000 genomes]
rs569593	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs570368	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[LWK][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs573044	0.96[CEU][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs575805	1.00[ASW][hapmap];0.96[CEU][hapmap];0.90[GIH][hapmap];0.81[LWK][hapmap];0.85[TSI][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6604080	0.88[CEU][hapmap]
rs6604082	0.91[CEU][hapmap];0.90[TSI][hapmap];0.90[ASN][1000 genomes]
rs6699855	0.84[ASW][hapmap]
rs7511656	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7511669	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7522081	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7529835	0.81[ASN][1000 genomes]
rs7533077	0.88[CEU][hapmap];0.82[TSI][hapmap]
rs7537221	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7542358	0.84[CEU][hapmap]
rs7542373	0.87[CEU][hapmap]
rs7545076	0.96[CEU][hapmap];0.81[MKK][hapmap];0.82[TSI][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs981583	0.87[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
8	nsv871508	chr1:92478130-92781579	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
9	nsv546821	chr1:92525678-92650349	ZNF genes & repeats Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs560389	ZNF326	cis	cerebellum	SCAN

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92609800-92651200	Weak transcription	Fetal Kidney	kidney
2	chr1:92625000-92648200	Weak transcription	Fetal Stomach	stomach
3	chr1:92625600-92651000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr1:92626200-92652000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr1:92626600-92648400	Weak transcription	Fetal Intestine Small	intestine
6	chr1:92626600-92650800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr1:92626600-92657400	Weak transcription	Right Ventricle	heart
8	chr1:92626800-92650000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:92626800-92651400	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr1:92627800-92648200	Weak transcription	Lung	lung
11	chr1:92628000-92648600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr1:92628200-92651800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr1:92632800-92648800	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr1:92633800-92649400	Weak transcription	HSMMtube	muscle
15	chr1:92635200-92650400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:92635600-92648400	Weak transcription	Rectal Smooth Muscle	rectum
17	chr1:92636200-92651000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr1:92636800-92652400	Weak transcription	Fetal Brain Female	brain
19	chr1:92637000-92647400	Weak transcription	Placenta	Placenta
20	chr1:92640200-92650200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:92640400-92649800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr1:92642400-92662600	Weak transcription	NHDF-Ad	bronchial
23	chr1:92644000-92647400	Strong transcription	Liver	Liver
24	chr1:92644800-92647400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr1:92645000-92648800	Weak transcription	Fetal Heart	heart
26	chr1:92645400-92649800	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr1:92645600-92649200	Weak transcription	Dnd41	blood
28	chr1:92645600-92650400	Weak transcription	Thymus	Thymus
29	chr1:92645800-92647400	Strong transcription	Primary hematopoietic stem cells	blood
30	chr1:92645800-92647400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr1:92645800-92647600	Strong transcription	Brain Anterior Caudate	brain
32	chr1:92645800-92648000	Strong transcription	Primary T cells from cord blood	blood
33	chr1:92645800-92648000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:92645800-92648000	Strong transcription	Adipose Nuclei	Adipose
35	chr1:92645800-92648000	Strong transcription	Brain Substantia Nigra	brain
36	chr1:92645800-92648200	Strong transcription	Left Ventricle	heart
37	chr1:92645800-92650200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr1:92646000-92647400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr1:92646000-92647400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:92646000-92647600	Strong transcription	Brain Hippocampus Middle	brain
41	chr1:92646000-92647600	Strong transcription	Fetal Brain Male	brain
42	chr1:92646200-92647400	Strong transcription	Brain Angular Gyrus	brain
43	chr1:92646400-92652000	Weak transcription	Psoas Muscle	Psoas
44	chr1:92646600-92648000	Strong transcription	Fetal Lung	lung
45	chr1:92646600-92651400	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr1:92646600-92652200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:92646800-92648000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr1:92646800-92651000	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr1:92646800-92652000	Weak transcription	Fetal Intestine Large	intestine
50	chr1:92647000-92648600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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