Variant report

Variant	rs12193698
Chromosome Location	chr6:167512073-167512074
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:167508063..167510526-chr6:167511244..167513696,2	K562	blood:
2	chr6:167511835..167514028-chr6:167517104..167518840,2	K562	blood:

Extended variants
information (count: 116 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs10484530	0.88[EUR][1000 genomes]
rs10484531	0.89[CHB][hapmap];0.84[JPT][hapmap]
rs1060404	0.94[CHB][hapmap]
rs10946204	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs10946207	0.89[CEU][hapmap];0.94[CHB][hapmap];0.84[EUR][1000 genomes]
rs10946208	0.80[EUR][1000 genomes]
rs10946212	0.83[AMR][1000 genomes]
rs10946213	0.84[AMR][1000 genomes]
rs10946214	0.84[AMR][1000 genomes]
rs10946215	0.84[AMR][1000 genomes]
rs10946216	0.89[CEU][hapmap]
rs12178491	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12203510	0.80[EUR][1000 genomes]
rs12208359	0.85[EUR][1000 genomes]
rs12209395	0.88[EUR][1000 genomes]
rs12523712	0.80[EUR][1000 genomes]
rs12528323	0.80[EUR][1000 genomes]
rs12528689	0.80[EUR][1000 genomes]
rs12529876	0.80[EUR][1000 genomes]
rs12529959	0.80[EUR][1000 genomes]
rs13195812	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs13204839	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13210649	0.80[EUR][1000 genomes]
rs13213249	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1358882	0.80[EUR][1000 genomes]
rs1358883	0.80[EUR][1000 genomes]
rs1407315	0.80[EUR][1000 genomes]
rs1571878	0.85[CEU][hapmap]
rs17524252	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17615336	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1810644	0.80[EUR][1000 genomes]
rs1854853	0.81[CEU][hapmap]
rs2001114	0.83[EUR][1000 genomes]
rs2001115	0.82[EUR][1000 genomes]
rs2038580	0.89[CHB][hapmap];0.84[JPT][hapmap];0.83[EUR][1000 genomes]
rs2039321	0.84[AMR][1000 genomes]
rs2237274	0.83[CHB][hapmap];0.84[JPT][hapmap]
rs2237276	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs2239823	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2239826	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2239827	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2285147	0.82[AMR][1000 genomes]
rs2285148	0.83[EUR][1000 genomes]
rs239935	0.94[CHB][hapmap]
rs3093024	0.88[CEU][hapmap]
rs3093025	0.84[CEU][hapmap]
rs427824	0.80[CHB][hapmap]
rs4710175	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4710176	0.83[EUR][1000 genomes]
rs4710178	0.85[AMR][1000 genomes]
rs4710179	0.85[AMR][1000 genomes]
rs4710181	0.85[AMR][1000 genomes]
rs4710182	0.85[AMR][1000 genomes]
rs4710183	0.85[AMR][1000 genomes]
rs4710185	0.80[CEU][hapmap]
rs6456149	0.80[EUR][1000 genomes]
rs6456150	0.80[EUR][1000 genomes]
rs6456151	0.80[EUR][1000 genomes]
rs6456152	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6900701	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs6902119	0.80[AMR][1000 genomes]
rs6904946	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs6905911	1.00[YRI][hapmap]
rs6907666	0.92[CEU][hapmap];0.85[EUR][1000 genomes]
rs6909502	0.80[EUR][1000 genomes]
rs6918286	0.80[AMR][1000 genomes]
rs6920858	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6921588	0.81[EUR][1000 genomes]
rs6923582	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs6932740	0.80[EUR][1000 genomes]
rs6934043	0.80[EUR][1000 genomes]
rs6936261	0.80[EUR][1000 genomes]
rs720325	0.80[EUR][1000 genomes]
rs7742305	0.82[EUR][1000 genomes]
rs7761977	0.82[EUR][1000 genomes]
rs7762156	0.82[EUR][1000 genomes]
rs7765739	0.81[AMR][1000 genomes]
rs7766242	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7774396	0.82[AMR][1000 genomes]
rs7775443	0.85[AMR][1000 genomes]
rs911632	0.80[EUR][1000 genomes]
rs916331	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9295385	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs9366089	0.85[AMR][1000 genomes]
rs9457249	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs9457251	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs9457252	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs9457256	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs9457260	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9457261	0.80[EUR][1000 genomes]
rs9457268	0.80[AMR][1000 genomes]
rs9457270	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9457273	1.00[YRI][hapmap];0.82[AMR][1000 genomes]
rs9459836	0.88[CHB][hapmap];0.83[JPT][hapmap]
rs9459838	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs9459841	0.94[CHB][hapmap];0.81[JPT][hapmap]
rs9459849	0.94[CHB][hapmap];0.84[JPT][hapmap]
rs9459854	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9459855	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9459862	0.81[EUR][1000 genomes]
rs9459872	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 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
15	nsv7997	chr6:167508594-167512568	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs12193698	RNASET2	cis	Whole Blood	GTEx
rs12193698	AL133458.1	cis	Whole Blood	GTEx

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167503600-167527200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:167508000-167512400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr6:167508200-167512200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:167508200-167512200	Weak transcription	Right Atrium	heart
5	chr6:167508400-167512200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr6:167508600-167512600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr6:167508600-167515200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr6:167509000-167512200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:167509000-167516400	Enhancers	Primary B cells from cord blood	blood
10	chr6:167509000-167525200	Enhancers	Primary B cells from peripheral blood	blood
11	chr6:167509200-167512200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr6:167509200-167512600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:167509400-167512200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr6:167509400-167512200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr6:167509400-167516000	Weak transcription	Stomach Mucosa	stomach
16	chr6:167509600-167512200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr6:167509600-167512200	Weak transcription	Fetal Thymus	thymus
18	chr6:167509800-167512200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr6:167509800-167512200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr6:167509800-167512400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr6:167509800-167513400	Enhancers	GM12878-XiMat	blood
22	chr6:167509800-167516200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr6:167510000-167516600	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr6:167511200-167517400	Weak transcription	Primary hematopoietic stem cells	blood
25	chr6:167511400-167512200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr6:167511400-167513200	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr6:167511600-167513200	Enhancers	Primary T cells fromperipheralblood	blood
28	chr6:167511800-167512800	Enhancers	Spleen	Spleen
29	chr6:167511800-167513200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr6:167511800-167513400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr6:167511800-167513400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr6:167511800-167513400	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr6:167511800-167513600	Enhancers	Placenta Amnion	Placenta Amnion
34	chr6:167512000-167512400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:167512000-167512800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr6:167512000-167513200	Enhancers	Primary T cells from cord blood	blood
37	chr6:167512000-167513200	Enhancers	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links