Variant report

Variant	rs6741567
Chromosome Location	chr2:152578014-152578015
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10180065	0.85[ASN][1000 genomes]
rs10185966	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11682909	1.00[CEU][hapmap]
rs11894672	1.00[CEU][hapmap]
rs11896217	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12464543	0.82[ASN][1000 genomes]
rs12693116	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1523181	1.00[CEU][hapmap]
rs16830418	1.00[CEU][hapmap]
rs2030588	1.00[CEU][hapmap]
rs3768658	1.00[CEU][hapmap]
rs3922996	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3922997	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4233654	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4266011	0.86[AFR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4306714	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4393745	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4414677	0.85[ASN][1000 genomes]
rs4450595	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4453694	1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4510224	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4552188	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4605370	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4664066	1.00[CEU][hapmap]
rs4664499	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59444636	0.82[ASN][1000 genomes]
rs6433590	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6433680	1.00[CEU][hapmap]
rs6711382	0.81[ASN][1000 genomes]
rs6715027	0.84[ASN][1000 genomes]
rs6715607	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6716286	0.80[ASN][1000 genomes]
rs6740508	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6743968	1.00[CEU][hapmap]
rs6749823	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6755393	1.00[CEU][hapmap]
rs6759419	0.86[AFR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7557801	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7563441	0.82[ASN][1000 genomes]
rs7564630	0.85[ASN][1000 genomes]
rs7581532	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7583060	0.85[ASN][1000 genomes]
rs7583148	0.85[ASN][1000 genomes]
rs9287998	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9288006	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934136	chr2:152308156-152664443	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1005746	chr2:152361972-153059840	Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv535984	chr2:152361972-153059840	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv933357	chr2:152526786-152591138	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152562200-152582000	Strong transcription	Fetal Muscle Trunk	muscle
2	chr2:152564600-152584000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr2:152575600-152580600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
4	chr2:152575600-152582000	Strong transcription	Fetal Muscle Leg	muscle
5	chr2:152575800-152580400	Genic enhancers	Skeletal Muscle Female	skeletal muscle
6	chr2:152575800-152584200	Weak transcription	Aorta	Aorta
7	chr2:152576800-152582000	Strong transcription	HSMMtube	muscle
8	chr2:152577400-152579200	Enhancers	Psoas Muscle	Psoas

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