Variant report

Variant	rs8065437
Chromosome Location	chr17:45721653-45721654
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:45717280..45719877-chr17:45720528..45723492,3	K562	blood:
2	chr17:45718911..45722559-chr17:45723248..45729310,6	MCF-7	breast:
3	chr17:45719437..45724233-chr17:45725184..45728657,6	MCF-7	breast:
4	chr17:45720454..45721979-chr17:45725237..45727987,2	K562	blood:

Variant related genes	Relation type
ENSG00000108424	Chromatin interaction
ENSG00000263766	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10163469	0.88[EUR][1000 genomes]
rs10853090	0.97[EUR][1000 genomes]
rs11079784	0.95[EUR][1000 genomes]
rs11650372	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11656855	0.97[EUR][1000 genomes]
rs11870935	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11871606	0.95[EUR][1000 genomes]
rs12150231	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12603290	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12937560	0.83[EUR][1000 genomes]
rs12943464	0.93[EUR][1000 genomes]
rs2317826	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3760370	0.94[EUR][1000 genomes]
rs3809868	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4092460	0.81[EUR][1000 genomes]
rs4239162	0.91[EUR][1000 genomes]
rs4239163	0.91[EUR][1000 genomes]
rs4264433	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4289035	0.96[EUR][1000 genomes]
rs4375701	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4399567	0.92[EUR][1000 genomes]
rs4580230	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4793842	0.89[EUR][1000 genomes]
rs4793908	0.91[EUR][1000 genomes]
rs4793913	0.90[EUR][1000 genomes]
rs4793978	0.95[EUR][1000 genomes]
rs4794001	0.97[EUR][1000 genomes]
rs4794016	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4794047	0.86[ASN][1000 genomes]
rs4794048	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55633793	0.93[EUR][1000 genomes]
rs56226803	0.94[EUR][1000 genomes]
rs62074014	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62074015	0.82[EUR][1000 genomes]
rs7207542	0.90[EUR][1000 genomes]
rs7210738	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7214799	0.81[EUR][1000 genomes]
rs7219303	0.94[EUR][1000 genomes]
rs7220935	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7223029	0.94[EUR][1000 genomes]
rs73315878	0.92[EUR][1000 genomes]
rs8065669	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8072100	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8075411	0.92[EUR][1000 genomes]
rs8077106	0.82[EUR][1000 genomes]
rs8078686	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8078880	0.92[EUR][1000 genomes]
rs8081717	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9891111	0.81[EUR][1000 genomes]
rs9905583	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9905922	0.93[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	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv525267	chr17:45451894-45735706	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	esv1811231	chr17:45520374-45764956	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' 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
4	esv1813964	chr17:45520374-45764956	Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats 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
5	esv2758458	chr17:45520374-45764956	Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats 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
6	esv2758693	chr17:45520374-45764956	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv428344	chr17:45520374-45764956	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs8065437	TBKBP1	cis	Artery Tibial	GTEx
rs8065437	KPNB1	Cis_1M	lymphoblastoid	RTeQTL
rs8065437	MRPL45P2	cis	Skin Sun Exposed Lower leg	GTEx
rs8065437	TBKBP1	cis	Nerve Tibial	GTEx

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45696600-45726000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr17:45696800-45726200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr17:45697000-45725800	Weak transcription	Brain Substantia Nigra	brain
4	chr17:45697200-45726000	Weak transcription	Brain Angular Gyrus	brain
5	chr17:45699400-45726000	Weak transcription	Brain Anterior Caudate	brain
6	chr17:45699400-45726200	Weak transcription	Fetal Kidney	kidney
7	chr17:45700000-45725600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr17:45700000-45725800	Weak transcription	Spleen	Spleen
9	chr17:45700400-45725800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr17:45700600-45725200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr17:45701400-45724800	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr17:45701400-45725600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr17:45701400-45725800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr17:45701400-45725800	Weak transcription	Left Ventricle	heart
15	chr17:45701400-45726000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr17:45701800-45723800	Weak transcription	Lung	lung
17	chr17:45701800-45725600	Weak transcription	Thymus	Thymus
18	chr17:45702000-45725800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr17:45702000-45726200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr17:45702200-45725800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr17:45702400-45725800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr17:45702600-45725800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr17:45702600-45725800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr17:45702600-45726000	Weak transcription	Brain Cingulate Gyrus	brain
25	chr17:45702800-45725800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr17:45702800-45725800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr17:45702800-45725800	Weak transcription	NHDF-Ad	bronchial
28	chr17:45702800-45726000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr17:45702800-45726000	Weak transcription	A549	lung
30	chr17:45702800-45726000	Weak transcription	HSMMtube	muscle
31	chr17:45703000-45724800	Weak transcription	Fetal Thymus	thymus
32	chr17:45703000-45725600	Weak transcription	Placenta	Placenta
33	chr17:45703600-45725800	Weak transcription	Brain Hippocampus Middle	brain
34	chr17:45704000-45726000	Weak transcription	Osteobl	bone
35	chr17:45704200-45724800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr17:45704400-45725800	Weak transcription	Stomach Smooth Muscle	stomach
37	chr17:45704600-45726000	Weak transcription	Colon Smooth Muscle	Colon
38	chr17:45705200-45726000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr17:45706000-45724800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr17:45708000-45725800	Weak transcription	Pancreas	Pancrea
41	chr17:45712000-45726000	Weak transcription	NHEK	skin
42	chr17:45712200-45725800	Weak transcription	HMEC	breast
43	chr17:45712400-45725800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr17:45712600-45725600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr17:45714000-45723800	Weak transcription	Primary B cells from cord blood	blood
46	chr17:45714000-45725200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr17:45714000-45725200	Weak transcription	Liver	Liver
48	chr17:45714000-45725800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr17:45714000-45725800	Weak transcription	Fetal Intestine Large	intestine
50	chr17:45714200-45724400	Weak transcription	Primary T helper cells fromperipheralblood	blood

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