Variant report

Variant	rs9498663
Chromosome Location	chr6:102116284-102116285
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10485273	0.91[CEU][hapmap];0.96[CHB][hapmap];0.91[JPT][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10872738	0.95[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap]
rs10872739	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1222958	0.95[CEU][hapmap];0.86[CHB][hapmap];0.82[JPT][hapmap];0.80[EUR][1000 genomes]
rs1222960	0.80[ASN][1000 genomes]
rs1337412	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1337415	0.83[CHB][hapmap];0.82[JPT][hapmap];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1337424	0.91[CHB][hapmap];0.87[JPT][hapmap];0.93[YRI][hapmap]
rs1415489	0.96[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes]
rs1832293	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1856133	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2065938	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs2105118	0.83[CHB][hapmap];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2225865	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2518294	0.92[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2518295	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2518303	0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2786251	0.95[CHB][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap]
rs2786254	0.91[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap]
rs2852560	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2852565	0.91[CHB][hapmap];0.91[JPT][hapmap];0.80[YRI][hapmap]
rs4839800	0.96[CHB][hapmap];0.91[JPT][hapmap]
rs6904687	0.89[CHB][hapmap];0.91[JPT][hapmap]
rs6923409	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap]
rs9322602	0.87[CHB][hapmap];0.95[JPT][hapmap];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9322603	0.87[CHB][hapmap];0.87[JPT][hapmap];0.82[YRI][hapmap]
rs9485526	0.91[CEU][hapmap];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9485530	0.91[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9485532	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9498658	0.91[CEU][hapmap];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9498659	0.90[CEU][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9498662	0.91[CEU][hapmap];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9498664	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9498667	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][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	nsv538392	chr6:101938381-102148360	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3384771	chr6:101996253-102283808	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1032499	chr6:102069885-102720998	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv463993	chr6:102084491-102165329	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv604317	chr6:102084491-102165329	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv527973	chr6:102114780-102119829	Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:102113600-102117000	Enhancers	HMEC	breast
2	chr6:102113600-102117600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:102114000-102116800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:102114000-102117000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:102114000-102117000	Enhancers	NHEK	skin
6	chr6:102114600-102121600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:102116000-102116800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr6:102116200-102118800	Enhancers	Pancreatic Islets	Pancreatic Islet

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