Variant report

Variant	rs16869175
Chromosome Location	chr5:90148010-90148011
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:90146751..90149071-chr5:90156624..90159516,2	K562	blood:
2	chr5:90146306..90149323-chr5:90149920..90152363,3	K562	blood:
3	chr5:90145396..90148045-chr5:90150505..90152535,3	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10045071	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10052015	0.83[CHB][hapmap]
rs10053303	0.88[CEU][hapmap];0.83[CHB][hapmap]
rs10059629	1.00[CEU][hapmap];0.92[CHB][hapmap];0.82[JPT][hapmap];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10060641	0.83[CHB][hapmap]
rs10075623	0.90[ASN][1000 genomes]
rs10078496	0.83[CHB][hapmap]
rs10474336	0.92[CHB][hapmap]
rs10514339	0.85[CHB][hapmap];1.00[CHD][hapmap]
rs10514340	0.88[CEU][hapmap]
rs12054681	0.83[CHB][hapmap]
rs12520956	0.83[CHB][hapmap]
rs12522395	0.92[CHB][hapmap]
rs13159353	0.97[ASN][1000 genomes]
rs2247415	0.92[CHB][hapmap];0.82[JPT][hapmap];0.96[ASN][1000 genomes]
rs2366935	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2438338	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2438342	1.00[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs2438343	0.92[CHB][hapmap];0.97[CHD][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs2438344	0.92[CHB][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs2438345	0.83[CHB][hapmap];0.97[CHD][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs2438351	0.92[CHB][hapmap]
rs2438353	0.92[CHB][hapmap];0.87[CHD][hapmap]
rs2443068	1.00[CHB][hapmap];0.93[CHD][hapmap];0.85[ASN][1000 genomes]
rs3098356	1.00[CHB][hapmap];0.97[CHD][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs4916698	0.88[CEU][hapmap];0.83[CHB][hapmap]
rs4916827	1.00[CHB][hapmap];0.90[CHD][hapmap]
rs4916829	1.00[CHB][hapmap];0.90[CHD][hapmap]
rs6865577	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6878896	0.83[CHB][hapmap]
rs6890101	0.90[ASN][1000 genomes]
rs7724016	0.83[CHB][hapmap]
rs881289	0.89[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	nsv517049	chr5:90003131-90262475	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs16869175	GPR98	cis	brain	BrainEAC

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90110200-90149600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr5:90112000-90151200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr5:90112000-90160600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr5:90112000-90175800	Weak transcription	Fetal Brain Female	brain
5	chr5:90137400-90148800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr5:90138000-90148600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr5:90142400-90149600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr5:90142400-90156200	Weak transcription	Fetal Brain Male	brain
9	chr5:90142600-90162400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:90144600-90148200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:90145200-90153400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr5:90145600-90149400	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr5:90145600-90153200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr5:90146200-90148600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr5:90146200-90149400	Weak transcription	K562	blood
16	chr5:90146600-90148400	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr5:90146800-90152600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:90147800-90149600	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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