Variant report

Variant	rs7958975
Chromosome Location	chr12:44721067-44721068
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10506245	1.00[ASN][1000 genomes]
rs1098497	1.00[ASN][1000 genomes]
rs12828607	1.00[CHB][hapmap]
rs1527315	1.00[ASN][1000 genomes]
rs1622682	1.00[ASN][1000 genomes]
rs1625442	1.00[ASN][1000 genomes]
rs1643432	1.00[ASN][1000 genomes]
rs1643433	1.00[ASN][1000 genomes]
rs1643434	1.00[ASN][1000 genomes]
rs1644007	1.00[ASN][1000 genomes]
rs1644009	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs1644010	0.83[ASN][1000 genomes]
rs1644011	0.83[ASN][1000 genomes]
rs1644014	1.00[ASN][1000 genomes]
rs1716605	1.00[ASN][1000 genomes]
rs1716606	1.00[ASN][1000 genomes]
rs1726874	0.83[ASN][1000 genomes]
rs1726879	1.00[ASN][1000 genomes]
rs1726884	1.00[ASN][1000 genomes]
rs1726887	1.00[ASN][1000 genomes]
rs1726888	1.00[ASN][1000 genomes]
rs1726889	1.00[ASN][1000 genomes]
rs1726890	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1726900	1.00[ASN][1000 genomes]
rs1798020	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1798023	1.00[ASN][1000 genomes]
rs1798025	0.83[ASN][1000 genomes]
rs1798026	0.83[ASN][1000 genomes]
rs1798027	0.83[ASN][1000 genomes]
rs58802461	1.00[ASN][1000 genomes]
rs60441308	1.00[ASN][1000 genomes]
rs73274199	0.83[ASN][1000 genomes]
rs73276236	1.00[ASN][1000 genomes]
rs73276240	1.00[ASN][1000 genomes]
rs73276275	1.00[ASN][1000 genomes]
rs7979642	1.00[JPT][hapmap]
rs840764	1.00[ASN][1000 genomes]
rs840766	1.00[ASN][1000 genomes]
rs840767	1.00[ASN][1000 genomes]
rs840768	1.00[ASN][1000 genomes]
rs840772	0.83[ASN][1000 genomes]
rs840773	1.00[ASN][1000 genomes]
rs840774	1.00[ASN][1000 genomes]
rs859016	1.00[ASN][1000 genomes]
rs863482	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	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	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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44699000-44736000	Weak transcription	Pancreas	Pancrea
2	chr12:44699000-44782000	Weak transcription	Aorta	Aorta
3	chr12:44709200-44743200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:44712400-44765800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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