Variant report

Variant	rs6941355
Chromosome Location	chr6:167506238-167506239
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 91 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10946205	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs10946208	0.86[EUR][1000 genomes]
rs1130033	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs12203510	0.87[EUR][1000 genomes]
rs12213683	0.87[EUR][1000 genomes]
rs12523712	0.87[EUR][1000 genomes]
rs12527827	0.86[EUR][1000 genomes]
rs12528323	0.87[EUR][1000 genomes]
rs12528689	0.87[EUR][1000 genomes]
rs12529238	0.87[EUR][1000 genomes]
rs12529876	0.87[EUR][1000 genomes]
rs12529959	0.87[EUR][1000 genomes]
rs13208636	0.87[EUR][1000 genomes]
rs13210649	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13213249	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1358882	0.87[EUR][1000 genomes]
rs1358883	0.87[EUR][1000 genomes]
rs1407315	0.87[EUR][1000 genomes]
rs17615336	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1810644	0.87[EUR][1000 genomes]
rs1951459	0.80[ASN][1000 genomes]
rs2001114	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2001115	0.89[EUR][1000 genomes]
rs2017338	0.87[EUR][1000 genomes]
rs204295	0.95[ASN][1000 genomes]
rs2181058	0.87[EUR][1000 genomes]
rs2181059	0.85[ASN][1000 genomes]
rs2237277	1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs2239826	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2239827	0.80[EUR][1000 genomes]
rs2282860	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs2282861	1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs2285147	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2285148	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4710176	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62436765	0.82[EUR][1000 genomes]
rs6456143	0.84[ASN][1000 genomes]
rs6456149	0.87[EUR][1000 genomes]
rs6456150	0.87[EUR][1000 genomes]
rs6456151	0.87[EUR][1000 genomes]
rs6456153	0.86[EUR][1000 genomes]
rs6456154	0.86[EUR][1000 genomes]
rs6902119	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6907666	0.95[CHB][hapmap]
rs6909180	0.87[EUR][1000 genomes]
rs6909475	0.87[EUR][1000 genomes]
rs6909502	0.87[EUR][1000 genomes]
rs6918286	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6921588	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6925969	0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6932740	0.87[EUR][1000 genomes]
rs6934043	0.87[EUR][1000 genomes]
rs6936261	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs720325	0.87[EUR][1000 genomes]
rs7742305	0.89[EUR][1000 genomes]
rs7748224	0.83[EUR][1000 genomes]
rs7749278	1.00[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs7760495	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7761977	0.89[EUR][1000 genomes]
rs7762156	0.89[EUR][1000 genomes]
rs7766242	0.80[EUR][1000 genomes]
rs911632	0.87[EUR][1000 genomes]
rs933243	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs9347170	0.96[CHB][hapmap];0.96[JPT][hapmap];0.80[ASN][1000 genomes]
rs9355610	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs9366078	0.95[CHB][hapmap];0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs9457258	0.86[ASN][1000 genomes]
rs9457261	0.87[EUR][1000 genomes]
rs9457268	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9457270	0.81[EUR][1000 genomes]
rs9459835	1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs9459842	0.84[ASN][1000 genomes]
rs9459853	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9459862	0.88[EUR][1000 genomes]
rs9459871	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9459872	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9459874	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019381	chr6:167090236-167558598	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
2	nsv538541	chr6:167090236-167558598	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	nsv948634	chr6:167200671-167838993	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
4	nsv532074	chr6:167320656-167781977	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
5	nsv1031039	chr6:167324021-167741439	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
6	nsv538543	chr6:167324021-167741439	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	21 gene(s)	inside rSNPs	diseases
7	nsv1026972	chr6:167335031-167671042	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
8	esv2752099	chr6:167448181-167579102	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1018193	chr6:167491589-167797294	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv538544	chr6:167491589-167797294	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
11	nsv469673	chr6:167500376-167658532	Flanking Active TSS Genic enhancers Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv482439	chr6:167500376-167658532	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
13	esv2758094	chr6:167501204-167845935	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	esv2759492	chr6:167501204-168176733	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs6941355	AL133458.1	cis	Whole Blood	GTEx
rs6941355	RNASET2	cis	Whole Blood	GTEx
rs6941355	AL133458.1	cis	lung	GTEx

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167502800-167507400	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr6:167503200-167508000	Weak transcription	Gastric	stomach
3	chr6:167503200-167509800	Enhancers	Primary hematopoietic stem cells	blood
4	chr6:167503600-167506400	Enhancers	Primary T cells fromperipheralblood	blood
5	chr6:167503600-167506400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
6	chr6:167503600-167507200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr6:167503600-167507600	Weak transcription	Right Atrium	heart
8	chr6:167503600-167527200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr6:167503800-167506400	Enhancers	Primary T cells from cord blood	blood
10	chr6:167503800-167506600	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr6:167503800-167507400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr6:167504200-167506600	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr6:167504200-167506800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr6:167504200-167507000	Weak transcription	Adipose Nuclei	Adipose
15	chr6:167504200-167507200	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr6:167504200-167507400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr6:167504400-167507400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr6:167504600-167508000	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr6:167505200-167506400	Enhancers	Rectal Mucosa Donor 29	rectum
20	chr6:167505200-167507400	Enhancers	Fetal Muscle Trunk	muscle
21	chr6:167505200-167509800	Flanking Active TSS	GM12878-XiMat	blood
22	chr6:167505400-167506800	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr6:167505400-167507200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
24	chr6:167505600-167507000	Enhancers	Duodenum Mucosa	Duodenum
25	chr6:167505600-167507000	Weak transcription	Fetal Muscle Leg	muscle
26	chr6:167505600-167507400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr6:167505600-167509000	Flanking Active TSS	Primary B cells from cord blood	blood
28	chr6:167505800-167507400	Weak transcription	Right Ventricle	heart
29	chr6:167505800-167511800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr6:167506000-167507000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:167506000-167507600	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr6:167506000-167508000	Bivalent Enhancer	Fetal Thymus	thymus
33	chr6:167506000-167508200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
34	chr6:167506000-167508600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr6:167506000-167509000	Flanking Active TSS	Primary B cells from peripheral blood	blood
36	chr6:167506200-167506400	Bivalent Enhancer	Thymus	Thymus
37	chr6:167506200-167506600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
38	chr6:167506200-167506800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr6:167506200-167507000	Enhancers	Spleen	Spleen
40	chr6:167506200-167508200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
41	chr6:167506200-167509800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--

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