Variant report

Variant	rs1037820
Chromosome Location	chr3:67765635-67765636
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1037819	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11717401	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11720476	0.86[EUR][1000 genomes]
rs11924244	0.81[AMR][1000 genomes]
rs11924309	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11925909	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12630936	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1459904	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1459905	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1459906	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1459908	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1459909	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1459917	0.85[AFR][1000 genomes]
rs17046864	0.86[EUR][1000 genomes]
rs2125811	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2362439	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4856797	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4856798	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4856881	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4856882	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4856885	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55833751	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6548740	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6548748	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6802973	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7614322	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7617263	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7617448	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7627435	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7632493	0.94[EUR][1000 genomes]
rs7637890	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7649792	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9832460	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9843013	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9881852	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470638	chr3:67367341-67814738	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	esv3359258	chr3:67589615-67828274	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv3431366	chr3:67765553-67766139	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1037820	GPR27	cis	cerebellum	SCAN

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67705800-67776000	Weak transcription	Ovary	ovary
2	chr3:67721400-67800400	Weak transcription	Left Ventricle	heart
3	chr3:67764000-67765800	Enhancers	H1 Cell Line	embryonic stem cell
4	chr3:67764600-67765800	Enhancers	Placenta Amnion	Placenta Amnion
5	chr3:67764600-67769600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:67764800-67766400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:67765600-67765800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:67765600-67767000	Enhancers	Fetal Lung	lung

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