Variant report

Variant	rs1016659
Chromosome Location	chr12:42358562-42358563
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1009723	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1024700	0.82[EUR][1000 genomes]
rs10431604	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10748323	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10785320	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10785321	0.83[ASN][1000 genomes]
rs1226303	0.90[CEU][hapmap]
rs1233988	0.92[EUR][1000 genomes]
rs1233992	0.84[EUR][1000 genomes]
rs1233994	0.84[EUR][1000 genomes]
rs1233996	0.84[EUR][1000 genomes]
rs1234032	0.96[EUR][1000 genomes]
rs1234033	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1234034	0.96[EUR][1000 genomes]
rs1234035	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1234037	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1234038	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1234040	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1234052	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1234054	0.92[EUR][1000 genomes]
rs1463613	0.85[CEU][hapmap]
rs1628871	0.83[CEU][hapmap]
rs1732351	0.89[CEU][hapmap]
rs1732352	0.85[CEU][hapmap]
rs1882139	0.81[EUR][1000 genomes]
rs2012636	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2091678	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6582378	0.90[CEU][hapmap]
rs712106	0.85[CEU][hapmap]
rs7303028	0.90[CEU][hapmap]
rs7957081	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7958455	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7958582	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs824716	0.85[CEU][hapmap]
rs824724	0.85[CEU][hapmap]
rs824734	0.90[CEU][hapmap]
rs824738	0.80[CEU][hapmap]
rs844046	0.85[CEU][hapmap]
rs865420	0.90[CEU][hapmap]
rs917666	0.82[EUR][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	nsv430505	chr12:42297931-42720773	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv832387	chr12:42345541-42465505	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42355400-42361400	Weak transcription	Brain Anterior Caudate	brain
2	chr12:42356400-42361400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr12:42356400-42361600	Weak transcription	Fetal Intestine Large	intestine
4	chr12:42356400-42361600	Weak transcription	Fetal Muscle Leg	muscle
5	chr12:42356600-42359000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr12:42357400-42359800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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