Variant report

Variant	rs2076776
Chromosome Location	chr1:57317063-57317064
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1033637	0.87[AMR][1000 genomes]
rs1033729	0.93[AMR][1000 genomes]
rs1360151	0.87[ASN][1000 genomes]
rs1411012	0.87[ASN][1000 genomes]
rs1418471	0.87[ASN][1000 genomes]
rs2284951	0.87[ASN][1000 genomes]
rs3738563	0.98[ASN][1000 genomes]
rs601662	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs603154	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61766985	0.98[ASN][1000 genomes]
rs622299	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs629799	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs634144	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs635922	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs636879	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs647513	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs647962	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs648939	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs649798	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs658444	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6588656	0.87[ASN][1000 genomes]
rs6588657	0.87[ASN][1000 genomes]
rs659330	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs662377	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs664142	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6669054	0.98[ASN][1000 genomes]
rs668551	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs669444	0.92[AMR][1000 genomes]
rs6696110	0.87[ASN][1000 genomes]
rs671137	0.92[AMR][1000 genomes]
rs682584	0.92[AMR][1000 genomes]
rs706476	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7520004	0.85[ASN][1000 genomes]
rs7520006	0.85[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	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv1000266	chr1:57291371-57319480	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr1:57314400-57317400	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr1:57315800-57320000	Enhancers	HepG2	liver
3	chr1:57316400-57317200	Enhancers	Fetal Brain Female	brain
4	chr1:57316600-57317200	Enhancers	Fetal Brain Male	brain
5	chr1:57316600-57323200	Enhancers	Fetal Intestine Small	intestine
6	chr1:57317000-57317200	Enhancers	Liver	Liver

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