Variant report

Variant	rs58010475
Chromosome Location	chr9:3277889-3277890
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs10429463	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1147822	0.84[EUR][1000 genomes]
rs11998979	0.86[EUR][1000 genomes]
rs12004313	0.86[EUR][1000 genomes]
rs12004744	0.82[EUR][1000 genomes]
rs1443205	0.82[EUR][1000 genomes]
rs16916423	0.92[EUR][1000 genomes]
rs17658724	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17658838	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17715051	0.82[AMR][1000 genomes]
rs17715160	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17715317	0.95[EUR][1000 genomes]
rs17715329	0.89[EUR][1000 genomes]
rs2304928	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2920363	0.87[EUR][1000 genomes]
rs2920369	0.91[EUR][1000 genomes]
rs2920370	0.93[EUR][1000 genomes]
rs2920375	0.82[EUR][1000 genomes]
rs2920381	0.84[EUR][1000 genomes]
rs2920383	0.90[EUR][1000 genomes]
rs2986686	0.93[EUR][1000 genomes]
rs2986687	0.87[EUR][1000 genomes]
rs2986688	0.81[EUR][1000 genomes]
rs2986691	0.81[EUR][1000 genomes]
rs2986693	0.83[EUR][1000 genomes]
rs2986695	0.90[EUR][1000 genomes]
rs2986696	0.90[EUR][1000 genomes]
rs2986697	0.90[EUR][1000 genomes]
rs2986698	0.90[EUR][1000 genomes]
rs2986700	0.90[EUR][1000 genomes]
rs2986701	0.88[EUR][1000 genomes]
rs2986702	0.88[EUR][1000 genomes]
rs2986703	0.86[EUR][1000 genomes]
rs2991297	0.82[EUR][1000 genomes]
rs2991298	0.82[EUR][1000 genomes]
rs2991300	0.83[EUR][1000 genomes]
rs2991301	0.88[EUR][1000 genomes]
rs2991305	0.90[EUR][1000 genomes]
rs2991306	0.84[EUR][1000 genomes]
rs2991307	0.89[EUR][1000 genomes]
rs2991308	0.87[EUR][1000 genomes]
rs2991310	0.87[EUR][1000 genomes]
rs2991311	0.87[EUR][1000 genomes]
rs2991318	0.84[EUR][1000 genomes]
rs3012680	0.86[ASN][1000 genomes]
rs3012686	0.86[EUR][1000 genomes]
rs3012688	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3012693	0.92[EUR][1000 genomes]
rs3012694	0.81[EUR][1000 genomes]
rs3012695	0.93[EUR][1000 genomes]
rs3012696	0.93[EUR][1000 genomes]
rs3012700	0.91[EUR][1000 genomes]
rs3012701	0.88[EUR][1000 genomes]
rs3012705	0.83[EUR][1000 genomes]
rs3012707	0.86[EUR][1000 genomes]
rs3012710	0.88[EUR][1000 genomes]
rs3012712	0.81[EUR][1000 genomes]
rs4008965	0.88[EUR][1000 genomes]
rs41312820	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs506149	0.80[EUR][1000 genomes]
rs540859	0.81[EUR][1000 genomes]
rs57295144	0.89[EUR][1000 genomes]
rs576347	0.89[EUR][1000 genomes]
rs59378342	0.89[EUR][1000 genomes]
rs612198	0.86[EUR][1000 genomes]
rs617047	0.85[EUR][1000 genomes]
rs617992	0.90[EUR][1000 genomes]
rs619401	0.82[EUR][1000 genomes]
rs625941	0.83[EUR][1000 genomes]
rs633893	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs656686	0.81[EUR][1000 genomes]
rs658123	0.84[EUR][1000 genomes]
rs672271	0.80[ASN][1000 genomes]
rs7025201	0.87[EUR][1000 genomes]
rs7025328	0.91[EUR][1000 genomes]
rs7035429	0.84[EUR][1000 genomes]
rs7044448	0.94[EUR][1000 genomes]
rs72699004	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72699014	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72699023	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72699033	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72699037	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs72699039	0.94[EUR][1000 genomes]
rs72699050	0.86[EUR][1000 genomes]
rs72699051	0.90[EUR][1000 genomes]
rs7850999	0.84[EUR][1000 genomes]
rs7859468	0.88[EUR][1000 genomes]
rs7860020	0.88[EUR][1000 genomes]
rs7866129	0.81[EUR][1000 genomes]
rs7868041	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892086	chr9:3012276-3410838	Bivalent Enhancer ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv1032921	chr9:3139007-3502815	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv539940	chr9:3139007-3502815	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv466090	chr9:3237378-3349487	Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv613145	chr9:3237378-3349487	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1032529	chr9:3254763-3319778	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv539941	chr9:3254763-3319778	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:3220400-3287400	Weak transcription	Psoas Muscle	Psoas
2	chr9:3223600-3284800	Weak transcription	Spleen	Spleen
3	chr9:3226600-3289600	Weak transcription	Colon Smooth Muscle	Colon
4	chr9:3233600-3292600	Weak transcription	Pancreas	Pancrea
5	chr9:3234800-3294400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr9:3241400-3278000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr9:3242000-3278000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr9:3242200-3287800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr9:3243800-3279200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:3244200-3338400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr9:3246800-3287000	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr9:3251600-3292600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr9:3252800-3278600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:3254200-3285600	Weak transcription	Fetal Heart	heart
15	chr9:3255000-3293000	Weak transcription	Small Intestine	intestine
16	chr9:3255800-3292800	Weak transcription	Fetal Muscle Leg	muscle
17	chr9:3256800-3293400	Weak transcription	Right Ventricle	heart
18	chr9:3257000-3289000	Weak transcription	Fetal Brain Male	brain
19	chr9:3257200-3290200	Weak transcription	Brain Germinal Matrix	brain
20	chr9:3257200-3290200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr9:3257200-3290200	Weak transcription	Brain Substantia Nigra	brain
22	chr9:3257200-3294000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr9:3257200-3294400	Weak transcription	Duodenum Mucosa	Duodenum
24	chr9:3257400-3279000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr9:3257400-3289000	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr9:3257800-3285800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr9:3261400-3281400	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr9:3263000-3286800	Weak transcription	Liver	Liver
29	chr9:3263200-3278400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr9:3263200-3294200	Weak transcription	Fetal Lung	lung
31	chr9:3263200-3294600	Weak transcription	Esophagus	oesophagus
32	chr9:3263200-3297800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr9:3263800-3286600	Weak transcription	Brain Hippocampus Middle	brain
34	chr9:3265200-3280200	Weak transcription	Aorta	Aorta
35	chr9:3265200-3291000	Weak transcription	Stomach Smooth Muscle	stomach
36	chr9:3265400-3278000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr9:3265400-3287200	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr9:3265400-3293000	Weak transcription	Brain Angular Gyrus	brain
39	chr9:3265600-3292600	Weak transcription	Fetal Muscle Trunk	muscle
40	chr9:3265600-3332000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr9:3268600-3292000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr9:3270400-3287600	Weak transcription	Adipose Nuclei	Adipose
43	chr9:3270800-3292600	Weak transcription	Brain Anterior Caudate	brain
44	chr9:3271000-3289200	Weak transcription	Thymus	Thymus
45	chr9:3271000-3289600	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr9:3271400-3287200	Weak transcription	Left Ventricle	heart
47	chr9:3272000-3291000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr9:3272000-3292800	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr9:3272000-3302800	Weak transcription	Ovary	ovary
50	chr9:3272200-3280400	Weak transcription	HUES48 Cell Line	embryonic stem cell

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