Variant report

Variant	rs9912467
Chromosome Location	chr17:16465105-16465106
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1006561	1.00[EUR][1000 genomes]
rs16959784	1.00[EUR][1000 genomes]
rs16959831	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16959832	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16959849	1.00[EUR][1000 genomes]
rs28375510	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28375681	1.00[EUR][1000 genomes]
rs28481713	1.00[EUR][1000 genomes]
rs28482815	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57062804	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57088651	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57432974	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6502511	0.98[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6502512	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7211497	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7212777	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7214389	1.00[EUR][1000 genomes]
rs7218171	1.00[EUR][1000 genomes]
rs7218177	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7220797	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7220867	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7221073	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7222107	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73282666	1.00[EUR][1000 genomes]
rs73282673	1.00[EUR][1000 genomes]
rs73282675	1.00[EUR][1000 genomes]
rs73282678	1.00[EUR][1000 genomes]
rs73980200	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8066377	1.00[EUR][1000 genomes]
rs8068846	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8069772	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8069951	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9890785	1.00[EUR][1000 genomes]
rs9899370	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9900136	1.00[EUR][1000 genomes]
rs9900601	1.00[EUR][1000 genomes]
rs9902632	1.00[EUR][1000 genomes]
rs9912759	1.00[EUR][1000 genomes]
rs9916250	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
3	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
4	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
5	nsv1063764	chr17:16171649-16662914	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	120 gene(s)	inside rSNPs	diseases
6	nsv1061463	chr17:16245878-16490691	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
7	nsv543216	chr17:16245878-16490691	Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
8	nsv1058448	chr17:16389870-16926287	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16454600-16467600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr17:16454800-16467600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
3	chr17:16455000-16471200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr17:16455400-16468600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr17:16456400-16466600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr17:16456400-16467800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr17:16458800-16471600	Weak transcription	HUVEC	blood vessel
8	chr17:16459000-16466200	Weak transcription	Colonic Mucosa	Colon
9	chr17:16459200-16467600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr17:16459600-16471800	Weak transcription	Stomach Mucosa	stomach
11	chr17:16459800-16467400	Strong transcription	Brain Germinal Matrix	brain
12	chr17:16460200-16466200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr17:16460600-16467600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr17:16460800-16467000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr17:16460800-16468200	Strong transcription	Skeletal Muscle Male	skeletal muscle
16	chr17:16461200-16466200	Weak transcription	Psoas Muscle	Psoas
17	chr17:16461200-16471800	Weak transcription	Gastric	stomach
18	chr17:16461400-16466600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr17:16461400-16467400	Strong transcription	Brain Angular Gyrus	brain
20	chr17:16461400-16467800	Strong transcription	Brain Hippocampus Middle	brain
21	chr17:16461600-16467800	Strong transcription	Stomach Smooth Muscle	stomach
22	chr17:16461800-16467200	Strong transcription	Brain Substantia Nigra	brain
23	chr17:16461800-16468200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr17:16462000-16465200	Strong transcription	Fetal Thymus	thymus
25	chr17:16462000-16467800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr17:16462200-16465600	Weak transcription	Colon Smooth Muscle	Colon
27	chr17:16462200-16466400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr17:16462200-16467200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr17:16462200-16467600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr17:16462200-16470800	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr17:16462200-16471800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr17:16462200-16471800	Weak transcription	Esophagus	oesophagus
33	chr17:16462200-16471800	Weak transcription	Pancreas	Pancrea
34	chr17:16462400-16465200	Strong transcription	Fetal Intestine Large	intestine
35	chr17:16463000-16466000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr17:16463000-16466600	Weak transcription	Right Ventricle	heart
37	chr17:16463200-16466000	Weak transcription	NHEK	skin
38	chr17:16463200-16466200	Weak transcription	Fetal Muscle Leg	muscle
39	chr17:16463200-16466200	Weak transcription	Spleen	Spleen
40	chr17:16463200-16467800	Strong transcription	Ovary	ovary
41	chr17:16463200-16468400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr17:16463200-16470800	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr17:16463200-16471200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr17:16463200-16471600	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr17:16463400-16470800	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr17:16463400-16471000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr17:16463400-16471200	Weak transcription	Fetal Kidney	kidney
48	chr17:16463600-16467800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr17:16463800-16471000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr17:16464000-16467400	Strong transcription	Fetal Lung	lung

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