Variant report

Variant	rs10068473
Chromosome Location	chr5:89990545-89990546
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 104 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10036980	0.87[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10043836	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10045236	0.83[ASN][1000 genomes]
rs10058765	0.96[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10060365	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10060427	0.96[CEU][hapmap];0.81[CHB][hapmap];0.84[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10062714	0.96[CEU][hapmap];0.81[CHB][hapmap];0.84[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.85[TSI][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10062924	0.96[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10067181	0.87[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10072105	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs1014750	0.83[ASN][1000 genomes]
rs1028191	0.81[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1028192	0.84[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1033290	0.81[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1033291	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10514327	0.92[JPT][hapmap]
rs10514333	0.86[ASW][hapmap];0.81[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10942596	0.85[JPT][hapmap]
rs10942597	0.85[JPT][hapmap]
rs10942605	0.87[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10942606	0.90[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1160121	0.87[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.96[ASN][1000 genomes]
rs12187830	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12188928	1.00[ASW][hapmap];0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12516985	1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12655180	0.82[JPT][hapmap]
rs12657264	0.83[ASN][1000 genomes]
rs13153584	0.84[ASN][1000 genomes]
rs13167491	0.83[ASN][1000 genomes]
rs13185955	0.85[JPT][hapmap]
rs1533603	1.00[JPT][hapmap]
rs1673378	0.84[JPT][hapmap]
rs1673379	0.92[JPT][hapmap]
rs16868957	0.96[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1700510	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs1700511	0.92[JPT][hapmap]
rs1878878	0.81[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1988788	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1993474	0.87[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2176624	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2222242	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2366771	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs2366773	0.91[JPT][hapmap]
rs2366774	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs2366777	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs28517617	0.84[ASN][1000 genomes]
rs28550273	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28587199	0.85[ASN][1000 genomes]
rs3805483	0.92[JPT][hapmap]
rs3927265	0.86[CHD][hapmap];0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs4379236	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs490812	0.92[JPT][hapmap]
rs4916681	0.96[CEU][hapmap];0.81[CHB][hapmap];0.87[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.95[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4916684	0.81[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4916686	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4916813	0.81[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap]
rs4916815	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs498491	0.80[CHB][hapmap];0.92[JPT][hapmap]
rs499148	0.85[JPT][hapmap]
rs502596	0.92[JPT][hapmap]
rs603015	0.85[JPT][hapmap]
rs617379	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs618355	0.83[JPT][hapmap]
rs637442	0.92[JPT][hapmap]
rs6452904	0.87[ASN][1000 genomes]
rs6452905	0.87[ASN][1000 genomes]
rs6452906	0.87[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs645652	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs648430	0.85[JPT][hapmap]
rs6861525	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6863710	0.81[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6878447	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6878917	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs6881412	0.87[CHD][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6883872	0.91[JPT][hapmap]
rs6888355	0.91[JPT][hapmap]
rs688956	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs688960	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs6898209	1.00[JPT][hapmap]
rs7703530	0.82[ASN][1000 genomes]
rs7703588	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7714506	0.85[ASN][1000 genomes]
rs7721198	1.00[JPT][hapmap]
rs7723259	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs7724806	1.00[JPT][hapmap]
rs7726624	0.81[CHB][hapmap];0.92[JPT][hapmap]
rs7729703	0.81[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7732169	0.87[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs9293550	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs963866	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs977906	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9790907	0.81[CHB][hapmap];0.92[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432750	chr5:89410113-90137144	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer 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	50 gene(s)	inside rSNPs	diseases
2	nsv432751	chr5:89457044-90090444	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529544	chr5:89523963-90412409	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv933668	chr5:89854253-89999672	Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv531965	chr5:89886550-90145002	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
6	nsv1032225	chr5:89940489-89999954	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
7	nsv1025391	chr5:89943364-89995164	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
8	nsv537805	chr5:89943364-89995164	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
9	nsv882367	chr5:89956991-90209824	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
10	nsv934323	chr5:89968158-90111853	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
11	nsv1015449	chr5:89968626-90219398	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
12	nsv882368	chr5:89990324-90012379	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10068473	GPR98	cis	cerebellum	SCAN

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89936800-89994200	Weak transcription	Brain Germinal Matrix	brain
2	chr5:89950400-90033400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr5:89964400-89993400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr5:89964600-89994800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:89965000-89993600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr5:89967200-89992000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:89979200-90002600	Weak transcription	Brain Anterior Caudate	brain
8	chr5:89981800-89992000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr5:89982000-90004600	Weak transcription	Fetal Brain Female	brain
10	chr5:89984200-89991800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:89985000-89994600	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr5:89985200-89991400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:89985200-89993000	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr5:89985600-89991000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr5:89985800-89990600	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr5:89985800-89991200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr5:89986800-89994200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:89987000-89991800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr5:89987000-89991800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:89987000-89991800	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr5:89987000-89992200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr5:89987000-90001200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr5:89987400-89991600	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr5:89987800-90007200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr5:89988800-89991200	Weak transcription	Lung	lung
26	chr5:89990400-89991800	Weak transcription	K562	blood
27	chr5:89990400-89992800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr5:89990400-89995400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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