Variant report

Variant	rs4921659
Chromosome Location	chr8:19400018-19400019
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10098467	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10107533	1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];0.91[ASN][1000 genomes]
rs1014481	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs1014482	0.91[ASN][1000 genomes]
rs10503650	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[TSI][hapmap];1.00[ASN][1000 genomes]
rs11781106	0.82[ASN][1000 genomes]
rs11784776	0.82[ASN][1000 genomes]
rs11994059	0.82[ASN][1000 genomes]
rs11994933	0.82[ASN][1000 genomes]
rs17128602	0.90[CEU][hapmap];1.00[CHB][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17128621	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.93[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17128626	0.91[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17128650	0.82[CEU][hapmap]
rs17408078	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs17408321	0.91[CEU][hapmap];1.00[CHB][hapmap];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17479581	0.82[ASN][1000 genomes]
rs17479749	0.82[ASN][1000 genomes]
rs17480050	1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];0.91[ASN][1000 genomes]
rs17480272	0.91[CEU][hapmap]
rs28522702	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs41332747	0.91[CEU][hapmap];0.95[GIH][hapmap];0.93[TSI][hapmap]
rs4921650	1.00[CHB][hapmap]
rs4922040	0.82[ASN][1000 genomes]
rs4922042	0.82[ASN][1000 genomes]
rs4922050	0.82[ASN][1000 genomes]
rs4922054	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs4922057	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4922060	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[GIH][hapmap];0.88[MEX][hapmap];0.89[TSI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4922061	0.82[CEU][hapmap]
rs55637382	0.82[ASN][1000 genomes]
rs55696969	1.00[ASN][1000 genomes]
rs55851368	0.82[ASN][1000 genomes]
rs55856414	0.82[ASN][1000 genomes]
rs55889457	0.82[ASN][1000 genomes]
rs56163568	0.82[ASN][1000 genomes]
rs57321774	0.82[ASN][1000 genomes]
rs7005625	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs73212558	0.82[ASN][1000 genomes]
rs73212568	0.82[ASN][1000 genomes]
rs73212569	0.82[ASN][1000 genomes]
rs73212582	0.82[ASN][1000 genomes]
rs73212595	1.00[ASN][1000 genomes]
rs73212598	1.00[ASN][1000 genomes]
rs73212600	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73212602	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73214608	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73214610	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73214611	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73214628	0.82[AMR][1000 genomes]
rs7818871	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533109	chr8:18845845-19456780	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv949636	chr8:18957705-19664732	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats 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	18 gene(s)	inside rSNPs	diseases
3	nsv948861	chr8:19199688-19609029	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv949304	chr8:19199688-19625912	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	esv34007	chr8:19252602-19482098	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv890624	chr8:19319061-19456270	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv610753	chr8:19364883-19439977	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv890625	chr8:19368697-19799641	Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	nsv1018057	chr8:19370830-19435399	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1016276	chr8:19374998-19435147	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1024012	chr8:19377703-19409791	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv890626	chr8:19383697-19483259	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv890627	chr8:19389865-19561997	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19379400-19434200	Weak transcription	Placenta	Placenta
2	chr8:19389000-19408000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr8:19390400-19408200	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr8:19395600-19402200	Weak transcription	Brain Hippocampus Middle	brain
5	chr8:19396200-19407800	Weak transcription	Primary T cells from cord blood	blood
6	chr8:19396400-19408800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr8:19396600-19405000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:19397600-19401000	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr8:19397600-19408200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr8:19398400-19400400	Weak transcription	Brain Anterior Caudate	brain
11	chr8:19398400-19404400	Weak transcription	Right Atrium	heart
12	chr8:19398400-19410400	Weak transcription	Aorta	Aorta
13	chr8:19398400-19411800	Weak transcription	Primary B cells from cord blood	blood
14	chr8:19398800-19408800	Weak transcription	Left Ventricle	heart
15	chr8:19399200-19400200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:19399200-19402000	Enhancers	A549	lung
17	chr8:19399400-19400200	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr8:19399800-19401000	Weak transcription	Hela-S3	cervix

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