Variant report

Variant	rs3774503
Chromosome Location	chr3:53677185-53677186
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs13059151	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13063116	0.87[CEU][hapmap]
rs13084908	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1380608	0.87[GIH][hapmap];1.00[MEX][hapmap]
rs17053285	1.00[JPT][hapmap]
rs17053295	1.00[JPT][hapmap]
rs17053338	0.93[GIH][hapmap]
rs17053363	0.93[GIH][hapmap]
rs2292918	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2633709	0.83[CHD][hapmap];1.00[JPT][hapmap]
rs2680657	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2680659	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs2946522	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35768922	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35989759	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs36036528	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3774482	0.87[CEU][hapmap]
rs3774483	1.00[JPT][hapmap]
rs3774485	1.00[JPT][hapmap]
rs3774487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3774488	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3774490	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3774496	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3774513	1.00[JPT][hapmap]
rs3821853	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs66596667	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6786894	0.87[CEU][hapmap]
rs6788419	0.83[CHD][hapmap];1.00[JPT][hapmap]
rs71301844	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs898412	1.00[JPT][hapmap]
rs898413	0.83[CHD][hapmap];1.00[JPT][hapmap]
rs898414	1.00[JPT][hapmap]

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	nsv1003621	chr3:53448934-54425322	Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv1001128	chr3:53659570-53927842	Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53652800-53684000	Weak transcription	Right Atrium	heart
2	chr3:53666400-53681400	Weak transcription	Fetal Lung	lung
3	chr3:53667600-53680600	Weak transcription	Fetal Intestine Large	intestine
4	chr3:53674800-53678000	Strong transcription	Fetal Intestine Small	intestine
5	chr3:53675200-53677600	Weak transcription	Esophagus	oesophagus
6	chr3:53676000-53677200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr3:53676200-53678000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr3:53676800-53688600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:53677000-53677200	Enhancers	Pancreatic Islets	Pancreatic Islet

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