Variant report

Variant	rs7224237
Chromosome Location	chr17:16535679-16535680
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11868291	0.88[EUR][1000 genomes]
rs11870650	0.85[EUR][1000 genomes]
rs2058197	0.83[EUR][1000 genomes]
rs28419755	0.83[EUR][1000 genomes]
rs28704561	0.83[EUR][1000 genomes]
rs59771043	0.86[EUR][1000 genomes]
rs62072767	0.85[EUR][1000 genomes]
rs62072768	0.83[EUR][1000 genomes]
rs62072769	0.85[EUR][1000 genomes]
rs62072771	0.86[EUR][1000 genomes]
rs62072776	0.88[EUR][1000 genomes]
rs62072777	0.88[EUR][1000 genomes]
rs62072778	0.88[EUR][1000 genomes]
rs62072782	1.00[EUR][1000 genomes]
rs62072783	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62072785	1.00[EUR][1000 genomes]
rs62072786	1.00[EUR][1000 genomes]
rs62072787	1.00[EUR][1000 genomes]
rs62072789	1.00[EUR][1000 genomes]
rs62072791	1.00[EUR][1000 genomes]
rs62072846	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62072847	1.00[EUR][1000 genomes]
rs62072856	1.00[EUR][1000 genomes]
rs62072857	1.00[EUR][1000 genomes]
rs62072858	1.00[EUR][1000 genomes]
rs62072859	1.00[EUR][1000 genomes]
rs62073662	1.00[EUR][1000 genomes]
rs62073663	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62073665	1.00[EUR][1000 genomes]
rs62073667	1.00[EUR][1000 genomes]
rs62073702	1.00[EUR][1000 genomes]
rs62073703	1.00[EUR][1000 genomes]
rs62073705	1.00[EUR][1000 genomes]
rs62073706	1.00[EUR][1000 genomes]
rs62073707	1.00[EUR][1000 genomes]
rs62073708	1.00[EUR][1000 genomes]
rs62073709	0.98[EUR][1000 genomes]
rs62073710	1.00[EUR][1000 genomes]
rs7218473	0.83[EUR][1000 genomes]
rs73982008	0.86[EUR][1000 genomes]
rs8065062	0.86[EUR][1000 genomes]
rs8065749	0.81[EUR][1000 genomes]
rs9899944	0.83[EUR][1000 genomes]
rs9902115	0.88[EUR][1000 genomes]
rs9909271	0.88[EUR][1000 genomes]
rs9909921	0.88[EUR][1000 genomes]
rs9910496	0.83[EUR][1000 genomes]

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	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	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
7	esv2758442	chr17:16527056-16817437	Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
8	esv2758676	chr17:16527056-16817437	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv427991	chr17:16527056-16817437	Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16519800-16540000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr17:16522000-16540000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr17:16523000-16540400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr17:16523400-16537000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr17:16523400-16538400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr17:16524600-16539400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr17:16525800-16538200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr17:16525800-16538400	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
9	chr17:16525800-16539800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr17:16527200-16542200	Weak transcription	Fetal Heart	heart
11	chr17:16527800-16537000	Weak transcription	Psoas Muscle	Psoas
12	chr17:16527800-16556000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr17:16528000-16536000	Weak transcription	NH-A	brain
14	chr17:16528000-16537600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr17:16528000-16556000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr17:16528600-16536800	Weak transcription	Fetal Brain Male	brain
17	chr17:16529000-16538000	Strong transcription	Fetal Lung	lung
18	chr17:16530000-16555400	Weak transcription	Small Intestine	intestine
19	chr17:16530200-16540000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr17:16531200-16538200	Strong transcription	Duodenum Smooth Muscle	Duodenum
21	chr17:16531200-16556200	Weak transcription	Right Ventricle	heart
22	chr17:16531400-16535800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr17:16531600-16543800	Weak transcription	Stomach Mucosa	stomach
24	chr17:16531800-16538000	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr17:16531800-16538200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr17:16531800-16556000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr17:16532000-16536600	Weak transcription	HSMM	muscle
28	chr17:16532000-16538200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr17:16532200-16536600	Weak transcription	Colonic Mucosa	Colon
30	chr17:16532200-16537600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr17:16532200-16538800	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr17:16532200-16556000	Weak transcription	NHLF	lung
33	chr17:16532400-16556600	Weak transcription	Lung	lung
34	chr17:16532600-16537800	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr17:16532800-16537600	Strong transcription	Osteobl	bone
36	chr17:16532800-16538000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr17:16533000-16536600	Strong transcription	Skeletal Muscle Male	skeletal muscle
38	chr17:16533000-16538000	Strong transcription	Adipose Nuclei	Adipose
39	chr17:16533000-16538400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
40	chr17:16533000-16539800	ZNF genes & repeats	A549	lung
41	chr17:16533200-16538600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr17:16533400-16536000	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr17:16533400-16536000	Weak transcription	Fetal Thymus	thymus
44	chr17:16533400-16537400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr17:16533400-16538200	Strong transcription	Fetal Muscle Leg	muscle
46	chr17:16533400-16538400	Strong transcription	Primary B cells from peripheral blood	blood
47	chr17:16533400-16538400	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr17:16533400-16556000	Weak transcription	HUVEC	blood vessel
49	chr17:16533400-16556400	Weak transcription	Aorta	Aorta
50	chr17:16533600-16536400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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