Variant report

Variant	rs7658695
Chromosome Location	chr4:142036573-142036574
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10008705	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10016770	0.81[ASN][1000 genomes]
rs10029478	0.91[ASN][1000 genomes]
rs10519584	0.82[EUR][1000 genomes]
rs12509440	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13435125	0.91[ASN][1000 genomes]
rs1395668	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1395669	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1873370	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2321862	1.00[ASN][1000 genomes]
rs28417061	0.91[ASN][1000 genomes]
rs28457672	0.91[ASN][1000 genomes]
rs28628800	0.91[ASN][1000 genomes]
rs28667926	0.96[ASN][1000 genomes]
rs3913899	0.93[EUR][1000 genomes]
rs4267811	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4386678	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4613644	0.89[ASN][1000 genomes]
rs4629541	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4637487	0.93[EUR][1000 genomes]
rs4956512	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4956513	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4956514	0.95[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4956515	0.91[ASN][1000 genomes]
rs4956516	0.91[ASN][1000 genomes]
rs4956517	0.86[ASN][1000 genomes]
rs62324901	0.93[EUR][1000 genomes]
rs62324902	0.93[EUR][1000 genomes]
rs6537030	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6813119	1.00[ASN][1000 genomes]
rs6817313	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6826231	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6831578	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6853785	0.81[ASN][1000 genomes]
rs6856997	0.85[EUR][1000 genomes]
rs756170	0.89[ASN][1000 genomes]
rs7669929	0.83[ASN][1000 genomes]
rs7683490	0.93[EUR][1000 genomes]
rs7697519	0.93[EUR][1000 genomes]
rs9790672	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9790673	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[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	nsv880167	chr4:141616979-142092124	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv880169	chr4:142005573-142038481	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142013000-142040400	Weak transcription	Psoas Muscle	Psoas
2	chr4:142026200-142039200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:142028600-142042400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr4:142031800-142039200	Weak transcription	Fetal Stomach	stomach
5	chr4:142031800-142041800	Weak transcription	Left Ventricle	heart
6	chr4:142032400-142036800	Weak transcription	Fetal Heart	heart

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