Variant report

Variant	rs17587847
Chromosome Location	chr4:166519822-166519823
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10001116	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10001551	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10003429	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10006198	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10018347	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10034270	0.91[EUR][1000 genomes]
rs10517852	1.00[ASN][1000 genomes]
rs10517854	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13134998	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1459510	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1459511	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17046758	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17046824	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17046826	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17046827	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17046853	0.91[EUR][1000 genomes]
rs17046894	0.86[EUR][1000 genomes]
rs17046897	0.86[EUR][1000 genomes]
rs17503409	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17503436	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17503589	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17503652	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17587826	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17587875	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17587980	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17588001	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17588022	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17588043	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17588175	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17588244	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17588258	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17632054	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1914845	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2322119	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28366377	0.80[EUR][1000 genomes]
rs28493919	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28537958	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28569800	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28581927	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28630955	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28654153	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28673221	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4543072	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4690822	0.80[EUR][1000 genomes]
rs59204772	0.91[EUR][1000 genomes]
rs6536921	1.00[ASN][1000 genomes]
rs6837884	0.91[EUR][1000 genomes]
rs6854166	0.91[EUR][1000 genomes]
rs72689403	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689404	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689405	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689406	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689409	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689410	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689413	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689414	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689415	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689416	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689419	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689420	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689422	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689423	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689424	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689425	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689427	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689428	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72689439	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72689440	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72689441	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72689442	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs72689444	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72705441	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72705449	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72705451	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72705452	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72705454	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72705456	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72705458	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72705460	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9308109	0.91[EUR][1000 genomes]
rs9996760	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9999778	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830141	chr4:166502908-166689626	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr4:166503000-166523800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:166519800-166520000	Enhancers	Pancreas	Pancrea

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