Variant report

Variant	rs12613707
Chromosome Location	chr2:64031160-64031161
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10201844	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10207847	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11125985	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11125986	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12612549	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12612596	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13384707	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1362797	0.84[EUR][1000 genomes]
rs1440004	0.80[EUR][1000 genomes]
rs2054119	0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2302809	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs36042418	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4072113	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4359637	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4399712	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4671526	0.90[EUR][1000 genomes]
rs4671532	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6546025	0.90[EUR][1000 genomes]
rs6546026	0.92[EUR][1000 genomes]
rs6546027	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6546038	0.81[EUR][1000 genomes]
rs6546039	0.85[EUR][1000 genomes]
rs6705192	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6737855	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6746875	0.80[EUR][1000 genomes]
rs7426051	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7596262	0.80[EUR][1000 genomes]
rs9309356	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs998043	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[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	nsv834242	chr2:63891249-64045617	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1013375	chr2:63969820-64231550	ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 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	chr2:64020400-64032000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:64023600-64032800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:64029200-64032400	Weak transcription	Liver	Liver
4	chr2:64029200-64045200	Weak transcription	Adipose Nuclei	Adipose

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