Variant report

Variant	rs3843960
Chromosome Location	chr16:31905717-31905718
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10871460	0.86[EUR][1000 genomes]
rs11150650	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11150651	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12444740	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12599066	0.94[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12919368	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12924931	0.93[EUR][1000 genomes]
rs1506907	1.00[CEU][hapmap]
rs1827959	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1828131	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1857943	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2358778	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3843961	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3850114	1.00[CEU][hapmap];1.00[GIH][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3861268	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3861270	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3913868	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3913870	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3913871	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4026652	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4026653	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs4026654	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4402587	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4889517	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4889518	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4889563	1.00[CEU][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889565	1.00[CEU][hapmap];1.00[GIH][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4889567	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4889568	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4889569	1.00[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6565290	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6565291	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7185691	0.87[AFR][1000 genomes]
rs7197804	1.00[GIH][hapmap];0.84[LWK][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7200162	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.90[TSI][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7202831	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7203345	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7205034	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8048908	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs8056158	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs8058598	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8059500	1.00[CEU][hapmap];1.00[GIH][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8060276	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs8062514	1.00[CEU][hapmap]
rs9788838	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9921760	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9924259	0.82[ASW][hapmap];0.94[MKK][hapmap]
rs9928574	0.96[EUR][1000 genomes]
rs9928704	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];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	nsv1067321	chr16:31652036-31959992	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv918074	chr16:31669781-31935033	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
3	nsv1063037	chr16:31669981-31934894	Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv542903	chr16:31669981-31934894	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv1066522	chr16:31831196-31959992	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv1057300	chr16:31862900-31959992	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv833196	chr16:31897381-32068953	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	esv1850460	chr16:31905688-32097085	Strong transcription ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31887800-31907400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:31889400-31911600	ZNF genes & repeats	Primary B cells from cord blood	blood
3	chr16:31890200-31905800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr16:31892000-31910400	ZNF genes & repeats	GM12878-XiMat	blood
5	chr16:31892400-31905800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr16:31892800-31906000	Weak transcription	Psoas Muscle	Psoas
7	chr16:31893000-31913200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr16:31893200-31911800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr16:31893400-31911400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr16:31893400-31911800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr16:31893400-31912000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
12	chr16:31893600-31917800	Weak transcription	Colon Smooth Muscle	Colon
13	chr16:31895000-31908400	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr16:31895000-31909600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
15	chr16:31895800-31910200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
16	chr16:31896600-31910400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
17	chr16:31897600-31912000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
18	chr16:31898600-31905800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr16:31899600-31910200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr16:31900000-31908200	Strong transcription	Fetal Thymus	thymus
21	chr16:31900000-31911000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr16:31900000-31911400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr16:31900400-31908800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr16:31900600-31907400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr16:31900600-31907600	Strong transcription	Fetal Intestine Large	intestine
26	chr16:31900600-31908400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr16:31900800-31907000	Strong transcription	Rectal Smooth Muscle	rectum
28	chr16:31900800-31907600	Strong transcription	Fetal Muscle Leg	muscle
29	chr16:31900800-31907800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
30	chr16:31900800-31907800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr16:31900800-31908800	Strong transcription	Placenta	Placenta
32	chr16:31901000-31908600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr16:31901000-31908800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
34	chr16:31901200-31905800	Strong transcription	Sigmoid Colon	Sigmoid Colon
35	chr16:31901200-31907800	Strong transcription	Adipose Nuclei	Adipose
36	chr16:31901800-31908000	Strong transcription	Brain Inferior Temporal Lobe	brain
37	chr16:31902000-31906000	Weak transcription	NHLF	lung
38	chr16:31902000-31908000	Strong transcription	Primary neutrophils fromperipheralblood	blood
39	chr16:31902200-31905800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr16:31902200-31907000	Strong transcription	Rectal Mucosa Donor 29	rectum
41	chr16:31902200-31907600	Strong transcription	HepG2	liver
42	chr16:31902200-31908000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr16:31902200-31908600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr16:31902400-31906000	Weak transcription	NHDF-Ad	bronchial
45	chr16:31902400-31907800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr16:31902600-31906000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr16:31902600-31906600	Strong transcription	Pancreas	Pancrea
48	chr16:31902600-31907200	Strong transcription	Fetal Lung	lung
49	chr16:31902800-31907600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr16:31903000-31906200	Strong transcription	Cortex derived primary cultured neurospheres	brain

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