Variant report

Variant	rs17020243
Chromosome Location	chr1:104713615-104713616
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10494009	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12723894	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12726311	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12731134	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12734586	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12739485	1.00[ASN][1000 genomes]
rs12741692	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12747868	0.82[ASN][1000 genomes]
rs12747997	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12755626	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12756615	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17019758	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17020242	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17020850	0.82[ASN][1000 genomes]
rs1887911	1.00[CHB][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1887912	1.00[ASN][1000 genomes]
rs1887913	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1887914	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1928332	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1928333	0.82[ASN][1000 genomes]
rs2094634	0.82[ASN][1000 genomes]
rs34020934	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34116274	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34292642	1.00[ASN][1000 genomes]
rs34292719	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34350097	0.82[ASN][1000 genomes]
rs34396730	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34413358	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34472079	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34536383	0.82[ASN][1000 genomes]
rs34610575	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs34769951	0.82[ASN][1000 genomes]
rs34861188	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35090280	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35137991	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35300832	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35719725	0.82[ASN][1000 genomes]
rs35726812	0.82[ASN][1000 genomes]
rs35976293	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs36012007	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs61091045	0.82[ASN][1000 genomes]
rs6657905	0.82[ASN][1000 genomes]
rs6689529	0.82[ASN][1000 genomes]
rs71655859	0.82[ASN][1000 genomes]
rs71669406	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs71669407	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs71669410	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs71669411	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7514438	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7515655	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7552164	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7556168	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9659160	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9662118	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9662847	0.80[AMR][1000 genomes];0.82[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	nsv1014507	chr1:104307231-104784753	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1012931	chr1:104322484-104778961	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv872072	chr1:104470622-105076810	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1010903	chr1:104483363-105468941	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv872073	chr1:104502333-104719055	Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv482341	chr1:104589525-104731812	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:104713000-104714800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:104713600-104713800	Enhancers	Fetal Heart	heart

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