Variant report

Variant	rs982003
Chromosome Location	chr10:18707296-18707297
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:18706370..18708448-chr10:18711471..18713680,2	MCF-7	breast:

Extended variants
information (count: 46 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10734052	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10734054	0.83[ASN][1000 genomes]
rs10734056	0.83[ASN][1000 genomes]
rs10741057	0.83[ASN][1000 genomes]
rs10741058	0.88[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.83[ASN][1000 genomes]
rs10741059	0.83[ASN][1000 genomes]
rs10741060	0.83[ASN][1000 genomes]
rs10741061	1.00[JPT][hapmap];0.85[MEX][hapmap];0.83[ASN][1000 genomes]
rs10764483	1.00[JPT][hapmap];0.85[MEX][hapmap];0.83[ASN][1000 genomes]
rs10828623	1.00[JPT][hapmap]
rs10828679	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.97[ASN][1000 genomes]
rs11014125	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11014185	0.90[ASN][1000 genomes]
rs11014186	0.90[ASN][1000 genomes]
rs11014196	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1575835	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1575836	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[ASN][1000 genomes]
rs1926026	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[ASN][1000 genomes]
rs1998820	1.00[CHB][hapmap]
rs2209587	0.86[ASN][1000 genomes]
rs2209588	0.81[ASN][1000 genomes]
rs2209589	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2209590	0.86[ASN][1000 genomes]
rs4748464	0.90[ASN][1000 genomes]
rs4748465	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4748468	1.00[CHB][hapmap]
rs6415973	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6415974	0.83[ASN][1000 genomes]
rs6482397	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6482406	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6482408	0.83[ASN][1000 genomes]
rs6482409	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6482412	0.86[ASN][1000 genomes]
rs6482437	0.83[ASN][1000 genomes]
rs7071123	0.83[ASN][1000 genomes]
rs7074324	0.82[AFR][1000 genomes]
rs7077248	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[MEX][hapmap];0.86[ASN][1000 genomes]
rs7083121	0.81[AFR][1000 genomes]
rs7095057	0.83[ASN][1000 genomes]
rs7893279	1.00[CHB][hapmap]
rs7912753	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs7923938	1.00[CHB][hapmap]
rs983048	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs997264	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv550042	chr10:18683267-18994583	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer 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	16 gene(s)	inside rSNPs	diseases
2	nsv1053675	chr10:18703895-18722912	Enhancers Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs982003	ITGA8	cis	cerebellum	SCAN

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18690200-18713000	Weak transcription	Ovary	ovary
2	chr10:18692000-18712600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr10:18692600-18707600	Weak transcription	Brain Angular Gyrus	brain
4	chr10:18702800-18707600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr10:18703200-18711200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr10:18703600-18732000	Weak transcription	Pancreas	Pancrea
7	chr10:18707000-18707400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr10:18707200-18707600	Weak transcription	Left Ventricle	heart
9	chr10:18707200-18708200	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr10:18707200-18708800	Enhancers	Fetal Heart	heart

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