Variant report

Variant	rs1798026
Chromosome Location	chr12:44683429-44683430
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10506245	0.83[ASN][1000 genomes]
rs1098497	0.83[ASN][1000 genomes]
rs1527315	0.83[ASN][1000 genomes]
rs1622682	0.83[ASN][1000 genomes]
rs1625442	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1643432	0.83[ASN][1000 genomes]
rs1643433	0.83[ASN][1000 genomes]
rs1643434	0.83[ASN][1000 genomes]
rs1644007	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1644009	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1644010	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1644011	1.00[ASN][1000 genomes]
rs1644014	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1716605	0.83[ASN][1000 genomes]
rs1716606	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1726874	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1726879	0.83[ASN][1000 genomes]
rs1726884	0.83[ASN][1000 genomes]
rs1726887	0.83[ASN][1000 genomes]
rs1726888	0.83[ASN][1000 genomes]
rs1726889	0.83[ASN][1000 genomes]
rs1726890	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1726900	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1798020	0.83[ASN][1000 genomes]
rs1798023	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1798025	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1798027	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58802461	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs60441308	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73274199	1.00[ASN][1000 genomes]
rs73276236	0.83[ASN][1000 genomes]
rs73276240	0.83[ASN][1000 genomes]
rs73276275	0.83[ASN][1000 genomes]
rs7958975	0.83[ASN][1000 genomes]
rs840764	0.83[ASN][1000 genomes]
rs840766	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs840767	0.83[ASN][1000 genomes]
rs840768	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs840773	0.83[ASN][1000 genomes]
rs840774	0.83[ASN][1000 genomes]
rs859016	0.83[ASN][1000 genomes]
rs863482	0.83[ASN][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	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv832393	chr12:44529406-44692414	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv686	chr12:44671240-44696910	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription	lncRNA	n/a	inside rSNPs	n/a
4	nsv1038498	chr12:44679455-44816572	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44676600-44697800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr12:44681200-44684000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:44682000-44698600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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