Variant report

Variant	rs17128535
Chromosome Location	chr8:19367972-19367973
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10087317	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10087663	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10088450	1.00[AMR][1000 genomes]
rs10094142	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10096485	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs10096490	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10096638	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10096712	1.00[YRI][hapmap]
rs10097851	1.00[AMR][1000 genomes]
rs10098690	1.00[YRI][hapmap]
rs10101907	1.00[AMR][1000 genomes]
rs10104266	1.00[YRI][hapmap]
rs10104615	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10104968	1.00[AMR][1000 genomes]
rs10105670	1.00[YRI][hapmap]
rs10106180	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10106270	1.00[AMR][1000 genomes]
rs10107181	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10109345	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10156383	1.00[YRI][hapmap]
rs10216575	1.00[YRI][hapmap]
rs10216916	1.00[YRI][hapmap]
rs13328370	1.00[YRI][hapmap]
rs17128349	1.00[YRI][hapmap]
rs17128520	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17128532	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17128545	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17128641	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17128662	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17128691	1.00[AMR][1000 genomes]
rs17128714	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs17128743	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs17128745	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs17128753	1.00[MEX][hapmap]
rs17128757	1.00[MEX][hapmap]
rs17128783	1.00[MEX][hapmap]
rs17128811	1.00[MEX][hapmap]
rs28415838	1.00[AMR][1000 genomes]
rs28427117	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28457744	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28491635	1.00[AMR][1000 genomes]
rs28578312	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28607676	1.00[AMR][1000 genomes]
rs28661517	1.00[AMR][1000 genomes]
rs28713671	1.00[AMR][1000 genomes]
rs28738093	1.00[AMR][1000 genomes]
rs28742998	1.00[AMR][1000 genomes]
rs7817946	1.00[AMR][1000 genomes]
rs7821215	1.00[AMR][1000 genomes]
rs7821389	1.00[AMR][1000 genomes]
rs7821612	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs7824941	1.00[AMR][1000 genomes]
rs7839912	1.00[AMR][1000 genomes]
rs7840172	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs7843893	1.00[AMR][1000 genomes]
rs9325858	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015395	chr8:18489538-19370258	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv429907	chr8:18578720-19398220	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv533109	chr8:18845845-19456780	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers 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 target site	20 gene(s)	inside rSNPs	diseases
4	nsv949636	chr8:18957705-19664732	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer 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	18 gene(s)	inside rSNPs	diseases
5	nsv948861	chr8:19199688-19609029	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv949304	chr8:19199688-19625912	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription 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 target site	11 gene(s)	inside rSNPs	diseases
7	esv34007	chr8:19252602-19482098	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
8	nsv890623	chr8:19307051-19383697	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv890624	chr8:19319061-19456270	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv610753	chr8:19364883-19439977	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19338800-19370600	Weak transcription	Esophagus	oesophagus
2	chr8:19348000-19376600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr8:19351200-19369000	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr8:19356000-19368400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr8:19356400-19368600	Weak transcription	Thymus	Thymus
6	chr8:19362800-19368400	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr8:19363000-19369600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr8:19363000-19372600	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr8:19363200-19368200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr8:19363200-19372800	Weak transcription	Spleen	Spleen
11	chr8:19363200-19376600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:19363400-19368400	Enhancers	Primary T cells from cord blood	blood
13	chr8:19363400-19368400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr8:19363400-19368400	Weak transcription	Gastric	stomach
15	chr8:19363400-19368400	Weak transcription	Pancreas	Pancrea
16	chr8:19363800-19368400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr8:19364200-19368400	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr8:19364200-19368600	Weak transcription	Primary neutrophils fromperipheralblood	blood
19	chr8:19364400-19368000	Weak transcription	Adipose Nuclei	Adipose
20	chr8:19364600-19368000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr8:19364600-19368400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr8:19364600-19368400	Weak transcription	Left Ventricle	heart
23	chr8:19364800-19376400	Weak transcription	Hela-S3	cervix
24	chr8:19365000-19368600	Weak transcription	Primary B cells from cord blood	blood
25	chr8:19365400-19372400	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr8:19365600-19368400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr8:19365600-19368400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr8:19365800-19372400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr8:19366000-19368400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr8:19366400-19368600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr8:19366600-19370600	Enhancers	Fetal Lung	lung
32	chr8:19366600-19370800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr8:19366600-19372400	Enhancers	Primary T cells fromperipheralblood	blood
34	chr8:19367000-19385000	Weak transcription	Ovary	ovary
35	chr8:19367200-19368600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
36	chr8:19367200-19370800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr8:19367400-19369200	Enhancers	Primary hematopoietic stem cells	blood
38	chr8:19367400-19370800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr8:19367600-19368200	Weak transcription	Fetal Thymus	thymus
40	chr8:19367600-19368400	Strong transcription	A549	lung
41	chr8:19367600-19368800	Enhancers	Brain Anterior Caudate	brain
42	chr8:19367600-19369000	Enhancers	Brain Angular Gyrus	brain
43	chr8:19367600-19369000	Enhancers	Brain Cingulate Gyrus	brain
44	chr8:19367600-19369000	Enhancers	Brain Hippocampus Middle	brain
45	chr8:19367600-19369000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr8:19367600-19370600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr8:19367800-19368000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:19367800-19368000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:19367800-19368200	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr8:19367800-19368200	Weak transcription	Placenta	Placenta

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