Variant report

Variant	rs9399999
Chromosome Location	chr6:106879571-106879572
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10457145	0.90[ASN][1000 genomes]
rs10485149	0.91[CEU][hapmap];0.91[JPT][hapmap];0.82[YRI][hapmap];0.90[ASN][1000 genomes]
rs10872004	0.80[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs10872005	0.90[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs10872006	0.90[ASN][1000 genomes]
rs11152979	0.90[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs11152981	0.90[ASN][1000 genomes]
rs11152983	0.90[ASN][1000 genomes]
rs11152985	0.90[CEU][hapmap];0.92[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs11152986	0.90[ASN][1000 genomes]
rs11152987	0.90[ASN][1000 genomes]
rs11753894	0.88[ASN][1000 genomes]
rs11755265	0.91[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs11758088	0.90[ASN][1000 genomes]
rs11968388	0.80[YRI][hapmap]
rs12190458	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12191953	0.90[ASN][1000 genomes]
rs12192409	0.89[ASN][1000 genomes]
rs12193577	0.90[ASN][1000 genomes]
rs12195390	0.89[ASN][1000 genomes]
rs12195477	0.90[ASN][1000 genomes]
rs12196067	0.90[ASN][1000 genomes]
rs12197928	0.90[ASN][1000 genomes]
rs12200404	0.90[ASN][1000 genomes]
rs12200677	0.90[ASN][1000 genomes]
rs12201080	0.89[ASN][1000 genomes]
rs12206207	0.90[ASN][1000 genomes]
rs12207671	0.90[ASN][1000 genomes]
rs12209473	0.90[ASN][1000 genomes]
rs12210758	0.90[ASN][1000 genomes]
rs12213356	0.95[ASN][1000 genomes]
rs1340611	0.90[ASN][1000 genomes]
rs17066969	0.85[ASN][1000 genomes]
rs35530260	0.89[ASN][1000 genomes]
rs3889294	0.90[ASN][1000 genomes]
rs4141621	0.90[ASN][1000 genomes]
rs55974983	0.89[ASN][1000 genomes]
rs56122958	0.90[ASN][1000 genomes]
rs56131632	0.90[ASN][1000 genomes]
rs56137433	0.90[ASN][1000 genomes]
rs56265466	0.90[ASN][1000 genomes]
rs60854560	0.90[ASN][1000 genomes]
rs748351	0.90[ASN][1000 genomes]
rs7747422	0.90[CEU][hapmap];0.92[CHB][hapmap];0.89[JPT][hapmap];0.81[YRI][hapmap];0.90[ASN][1000 genomes]
rs9320163	0.91[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];0.90[ASN][1000 genomes]
rs9372127	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9373862	0.93[EUR][1000 genomes]
rs9373863	0.84[EUR][1000 genomes]
rs9386539	0.96[ASN][1000 genomes]
rs9399996	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9399997	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9399998	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9400003	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]

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	nsv932155	chr6:106281728-107030467	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv1025900	chr6:106529777-106898421	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1018270	chr6:106531658-106908606	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv538399	chr6:106531658-106908606	Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv532047	chr6:106591482-107143252	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	nsv1020047	chr6:106597828-106912047	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
7	nsv970664	chr6:106635267-106887670	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	nsv870375	chr6:106696090-107047892	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
9	nsv1025510	chr6:106791080-106982400	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv538404	chr6:106791080-106982400	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
11	nsv1031707	chr6:106803325-106896650	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
12	nsv970345	chr6:106871018-106894266	Bivalent Enhancer Enhancers Weak transcription Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:106853200-106896000	Weak transcription	Esophagus	oesophagus
2	chr6:106866000-106887800	Weak transcription	Pancreas	Pancrea
3	chr6:106871000-106879600	Weak transcription	HMEC	breast
4	chr6:106877400-106887800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr6:106877600-106879800	Enhancers	Fetal Intestine Large	intestine
6	chr6:106878600-106882000	Weak transcription	Fetal Intestine Small	intestine
7	chr6:106879200-106879800	Enhancers	Liver	Liver
8	chr6:106879200-106880200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:106879200-106880400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:106879200-106880600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:106879400-106880600	Genic enhancers	NHEK	skin

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