Variant report

Variant	rs9382286
Chromosome Location	chr6:53964670-53964671
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs12055520	1.00[CHB][hapmap]
rs12174563	1.00[CHB][hapmap]
rs12176530	1.00[CHB][hapmap]
rs526232	1.00[CHB][hapmap]
rs9349697	1.00[CHB][hapmap]
rs9357789	1.00[CHB][hapmap]
rs9357790	1.00[CHB][hapmap]
rs9357792	1.00[CHB][hapmap]
rs9367552	1.00[CHB][hapmap]
rs9370262	1.00[CHB][hapmap]
rs9370263	1.00[CHB][hapmap]
rs9370264	1.00[CHB][hapmap]
rs9370267	1.00[CHB][hapmap]
rs9370271	1.00[CHB][hapmap]
rs9370272	1.00[CHB][hapmap]
rs9370273	1.00[CHB][hapmap]
rs9370275	1.00[CHB][hapmap]
rs9382287	1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs9382293	1.00[CHB][hapmap]
rs9382296	1.00[CHB][hapmap]
rs9382297	1.00[CHB][hapmap]
rs9382298	1.00[CHB][hapmap]
rs9382310	1.00[CHB][hapmap]
rs9395903	1.00[CHB][hapmap]
rs9395906	1.00[CHB][hapmap]
rs9395907	1.00[CHB][hapmap]
rs9395909	1.00[CHB][hapmap]
rs9395912	1.00[CHB][hapmap]
rs9395913	1.00[CHB][hapmap]
rs9474735	1.00[CHB][hapmap]

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	nsv1067663	chr6:53796341-54449718	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv529158	chr6:53796341-54449718	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv2758055	chr6:53839373-53996093	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv2759431	chr6:53839373-54007349	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv603110	chr6:53885918-54103794	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv7901	chr6:53914491-53981080	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv823691	chr6:53918427-53978766	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv885885	chr6:53920024-54046264	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv34853	chr6:53924697-53977449	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv1017633	chr6:53935336-54118476	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	esv2757169	chr6:53951857-54007349	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv885886	chr6:53956877-54009067	Enhancers Genic enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv885887	chr6:53961784-54046264	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:53945000-53970800	Weak transcription	Right Atrium	heart
2	chr6:53959400-53975800	Weak transcription	Fetal Muscle Leg	muscle
3	chr6:53959800-53967000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:53960000-53965400	Weak transcription	Fetal Heart	heart
5	chr6:53961000-53966800	Weak transcription	Fetal Brain Male	brain
6	chr6:53961400-53967400	Weak transcription	Fetal Brain Female	brain
7	chr6:53961600-53965400	Weak transcription	Left Ventricle	heart
8	chr6:53961600-53966800	Weak transcription	Psoas Muscle	Psoas
9	chr6:53961600-53966800	Weak transcription	Right Ventricle	heart
10	chr6:53963800-53965400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr6:53964400-53965000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:53964600-53964800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr6:53964600-53965200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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