Variant report

Variant	rs73857778
Chromosome Location	chr4:150751118-150751119
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10015292	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10021417	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10022183	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10023718	1.00[EUR][1000 genomes]
rs10023988	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10030973	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10032786	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10213081	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13434843	0.86[AMR][1000 genomes]
rs1394846	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17026442	1.00[EUR][1000 genomes]
rs17026476	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17026503	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17026506	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17026559	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17026577	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2359689	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28390223	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28419623	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28461843	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28533652	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28545223	1.00[EUR][1000 genomes]
rs28566505	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28657505	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28695593	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28703191	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28709180	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4594705	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4835596	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4835603	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4835606	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6824353	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6831721	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72965326	1.00[EUR][1000 genomes]
rs73857791	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73857792	0.82[AMR][1000 genomes]
rs73857798	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73859805	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7655327	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7665522	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7667627	0.87[AMR][1000 genomes]
rs7677933	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7684559	0.93[AMR][1000 genomes]
rs7690612	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7692136	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9284658	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs967371	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9991476	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9998271	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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	nsv1026797	chr4:150246932-151217137	Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1016169	chr4:150670127-150903827	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv537299	chr4:150670127-150903827	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv880254	chr4:150712923-150852782	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150745800-150752800	Weak transcription	Hela-S3	cervix
2	chr4:150746800-150752200	Weak transcription	Muscle Satellite Cultured Cells	--

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