Variant report

Variant	rs2274584
Chromosome Location	chr6:70962039-70962040
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10806631	1.00[CEU][hapmap];0.92[GIH][hapmap];0.90[MEX][hapmap];0.89[TSI][hapmap];0.86[EUR][1000 genomes]
rs10806632	0.86[EUR][1000 genomes]
rs10945206	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10945209	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs10945210	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs11754328	0.91[JPT][hapmap]
rs11757395	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12154117	0.90[MEX][hapmap]
rs12189655	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs12191702	0.84[CEU][hapmap]
rs12192237	0.87[CEU][hapmap]
rs12193867	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs12195310	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs12195966	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs12196905	0.86[EUR][1000 genomes]
rs12201626	0.87[CEU][hapmap]
rs12205998	0.86[EUR][1000 genomes]
rs12210719	0.87[CEU][hapmap]
rs12210870	1.00[CEU][hapmap];0.88[GIH][hapmap];0.85[TSI][hapmap];0.86[EUR][1000 genomes]
rs12211880	0.85[CEU][hapmap]
rs1321059	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16868815	0.85[JPT][hapmap]
rs16868818	0.85[JPT][hapmap]
rs16868820	0.85[JPT][hapmap]
rs16868822	0.85[JPT][hapmap]
rs17581483	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2274586	0.95[EUR][1000 genomes]
rs3737010	0.85[JPT][hapmap]
rs3806074	0.84[JPT][hapmap]
rs3806076	0.85[JPT][hapmap]
rs3806089	0.85[JPT][hapmap]
rs55860958	0.86[EUR][1000 genomes]
rs6913123	0.85[JPT][hapmap]
rs72923164	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72923166	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72924908	0.86[EUR][1000 genomes]
rs883708	0.85[JPT][hapmap]
rs9354910	1.00[CEU][hapmap];0.92[GIH][hapmap];0.90[MEX][hapmap];0.96[TSI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9354911	1.00[CEU][hapmap];0.92[GIH][hapmap];0.90[MEX][hapmap];0.89[TSI][hapmap];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933674	chr6:70663616-70973112	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv886142	chr6:70741209-71251421	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv1027049	chr6:70961610-71561488	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh 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	29 gene(s)	inside rSNPs	diseases
5	nsv524328	chr6:70961833-71558805	Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	nsv917312	chr6:70961903-71601688	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2274584	LMBRD1	cis	parietal	SCAN
rs2274584	COL9A1	cis	cerebellum	SCAN

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70952200-70964600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:70952200-70980400	Weak transcription	Fetal Stomach	stomach
3	chr6:70952200-70990000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr6:70952600-70966600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr6:70952600-70980400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:70952800-70989800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr6:70955200-70971000	Weak transcription	Fetal Kidney	kidney
8	chr6:70961200-70968000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:70961400-70962200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:70962000-70983600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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