Variant report

Variant	rs1474119
Chromosome Location	chr5:90002885-90002886
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:89998991..90003482-chr5:90003758..90009177,7	K562	blood:
2	chr5:89996062..89998352-chr5:90001342..90003176,2	K562	blood:
3	chr5:90001746..90003482-chr5:90003758..90005802,2	K562	blood:
4	chr5:90001172..90003183-chr5:90006013..90008402,2	K562	blood:
5	chr5:89996062..89999170-chr5:90000730..90003176,4	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10035335	0.97[ASN][1000 genomes]
rs10037067	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10040165	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs10043564	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes]
rs10064606	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs10942604	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11958484	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs12186867	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.86[EUR][1000 genomes]
rs12653924	0.95[CEU][hapmap];0.85[EUR][1000 genomes]
rs1474120	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs149321	0.96[CEU][hapmap];0.91[TSI][hapmap];0.85[EUR][1000 genomes]
rs1568308	0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1673381	1.00[CEU][hapmap]
rs16868980	1.00[CHB][hapmap];0.97[CHD][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs16868999	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs16869010	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs16869042	0.91[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs16876822	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2366772	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs2366775	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs2366926	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs257847	0.96[CEU][hapmap];0.89[TSI][hapmap]
rs27197	0.96[CEU][hapmap];0.89[TSI][hapmap];0.84[EUR][1000 genomes]
rs28407508	0.89[ASN][1000 genomes]
rs28796004	0.96[ASN][1000 genomes]
rs3112773	0.83[EUR][1000 genomes]
rs35851488	0.91[ASN][1000 genomes]
rs3942393	0.94[ASN][1000 genomes]
rs4588621	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs4916683	0.92[ASN][1000 genomes]
rs4916685	0.91[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs5028525	0.96[CEU][hapmap];0.91[TSI][hapmap];0.86[EUR][1000 genomes]
rs55835641	0.90[ASN][1000 genomes]
rs56255871	0.90[ASN][1000 genomes]
rs56369423	0.96[ASN][1000 genomes]
rs62375106	0.85[ASN][1000 genomes]
rs649449	0.96[CEU][hapmap];0.89[TSI][hapmap];0.83[EUR][1000 genomes]
rs6861067	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6880239	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs6891840	0.84[EUR][1000 genomes]
rs6892132	0.96[CEU][hapmap];0.89[TSI][hapmap];0.85[EUR][1000 genomes]
rs6894453	0.86[ASN][1000 genomes]
rs7716829	1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs908818	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.86[EUR][1000 genomes]
rs970319	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	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
5	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
6	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
7	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
8	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
9	nsv1031718	chr5:89999033-90099868	Weak transcription Strong transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1474119	GPR98	cis	cerebellum	SCAN

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89950400-90033400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr5:89982000-90004600	Weak transcription	Fetal Brain Female	brain
3	chr5:89987800-90007200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr5:89991800-90014000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr5:89995000-90025800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr5:89997800-90017600	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:89998800-90018000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:89999600-90010000	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr5:89999800-90004200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:90001800-90006000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:90002000-90005600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr5:90002200-90012200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:90002200-90022000	Weak transcription	Brain Germinal Matrix	brain
14	chr5:90002200-90023200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr5:90002400-90005600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr5:90002800-90003000	Strong transcription	K562	blood

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