Variant report

Variant	rs72852924
Chromosome Location	chr2:144730856-144730857
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs12612842	0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs12618509	0.86[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs12619798	0.99[ASN][1000 genomes]
rs12621041	0.99[ASN][1000 genomes]
rs16823361	0.99[ASN][1000 genomes]
rs16823373	0.99[ASN][1000 genomes]
rs16823382	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1861878	0.83[AFR][1000 genomes]
rs1864245	0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs2111671	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28679451	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35790422	0.99[ASN][1000 genomes]
rs3755088	0.89[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs3820756	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs55634187	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56090763	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs56120346	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56123489	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs56136411	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs56166856	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56396630	0.92[AFR][1000 genomes]
rs58186643	0.93[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs60305932	0.93[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs61202373	0.99[ASN][1000 genomes]
rs72851896	0.99[ASN][1000 genomes]
rs72852907	0.93[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs72852908	0.99[ASN][1000 genomes]
rs72852911	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs72852913	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs72852918	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs72852926	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72852929	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72852930	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72852932	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72852936	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72852938	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72852941	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72852947	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72852948	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72852967	0.87[ASN][1000 genomes]
rs72852969	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs72852982	0.81[AMR][1000 genomes]
rs72852985	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs72852992	0.83[AFR][1000 genomes]
rs73962140	0.85[AFR][1000 genomes]
rs73962146	0.88[AFR][1000 genomes]
rs73962150	0.92[AFR][1000 genomes]
rs73962160	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7572132	0.99[ASN][1000 genomes]
rs787170	0.88[ASN][1000 genomes]
rs9678811	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532755	chr2:144631279-145270874	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv1006344	chr2:144657716-145334899	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv535951	chr2:144657716-145334899	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv1067624	chr2:144657717-145425705	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	nsv531413	chr2:144657717-145425705	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:144713600-144780000	Weak transcription	HSMMtube	muscle
2	chr2:144718200-144732000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:144723000-144795600	Weak transcription	Primary T cells from cord blood	blood
4	chr2:144723800-144742000	Weak transcription	Fetal Muscle Leg	muscle
5	chr2:144724600-144741800	Weak transcription	Fetal Lung	lung
6	chr2:144726200-144780800	Weak transcription	Primary B cells from cord blood	blood
7	chr2:144730800-144746200	Weak transcription	Primary hematopoietic stem cells	blood

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