Variant report

Variant	rs9809330
Chromosome Location	chr3:79006302-79006303
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1009682	0.80[EUR][1000 genomes]
rs1031933	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10514741	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13317939	0.85[AFR][1000 genomes]
rs13321050	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13321792	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13321973	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13325521	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17016641	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17016646	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17016648	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17016656	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28412538	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28667917	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28729472	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57432814	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58249522	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58608513	0.89[AFR][1000 genomes]
rs72906176	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72906179	0.82[EUR][1000 genomes]
rs72910206	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72910208	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72910211	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72910220	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72910224	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9631526	0.85[AFR][1000 genomes]
rs9818387	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9832632	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9833345	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9836486	0.82[AFR][1000 genomes]
rs9838831	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9842144	0.83[AFR][1000 genomes]
rs9845223	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9853126	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9858080	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9858480	0.82[EUR][1000 genomes]
rs9861490	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9868575	0.86[AFR][1000 genomes]
rs9870336	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9879944	0.86[AFR][1000 genomes]
rs9880690	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010804	chr3:78739648-79087470	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv533681	chr3:78750924-79017336	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv834744	chr3:78911545-79076470	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	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	chr3:79001000-79012400	Weak transcription	Fetal Stomach	stomach
2	chr3:79001000-79024200	Weak transcription	Colon Smooth Muscle	Colon
3	chr3:79002400-79006600	Weak transcription	Brain Substantia Nigra	brain
4	chr3:79002600-79010600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr3:79005200-79007200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:79005600-79007200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr3:79005800-79006600	Enhancers	Brain Cingulate Gyrus	brain
8	chr3:79005800-79007000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:79005800-79007000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:79005800-79007200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:79006000-79007000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:79006000-79007000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr3:79006000-79007200	Enhancers	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links