Variant report

Variant	rs13195749
Chromosome Location	chr6:145223626-145223627
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs11969748	0.91[ASN][1000 genomes]
rs12175408	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12175421	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13198108	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13201654	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13210332	0.82[ASN][1000 genomes]
rs13210889	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13217690	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1338696	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1338697	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1338704	0.95[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs1338705	0.91[ASN][1000 genomes]
rs1538401	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1538402	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2050719	0.90[ASN][1000 genomes]
rs2153108	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2153109	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2153110	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2185143	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35361162	0.82[AMR][1000 genomes]
rs4143178	0.81[EUR][1000 genomes]
rs4323328	0.81[ASN][1000 genomes]
rs4331996	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4331997	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4487599	0.90[ASN][1000 genomes]
rs4526219	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4637659	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4895660	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4896761	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4896762	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57337295	0.89[ASN][1000 genomes]
rs57590687	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62438853	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6570657	0.85[EUR][1000 genomes]
rs6570659	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6570660	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6570661	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6909971	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6910398	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6913165	0.89[ASN][1000 genomes]
rs6914560	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6931199	0.81[EUR][1000 genomes]
rs6934724	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6935054	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6935093	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6935178	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6935436	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7742815	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7742893	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7743204	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7762951	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7769009	0.82[CHB][hapmap]
rs7769065	0.90[ASN][1000 genomes]
rs9283117	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9321998	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9321999	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9322000	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9322001	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9322002	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9322005	0.90[ASN][1000 genomes]
rs9373433	0.88[ASN][1000 genomes]
rs9373434	0.96[ASN][1000 genomes]
rs9376873	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9376874	0.90[ASN][1000 genomes]
rs9376877	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9386088	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9386089	0.88[ASN][1000 genomes]
rs9390249	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9390250	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9390251	0.90[ASN][1000 genomes]
rs9390252	0.89[ASN][1000 genomes]
rs9390253	0.89[ASN][1000 genomes]
rs9390254	0.88[ASN][1000 genomes]
rs9390257	0.96[ASN][1000 genomes]
rs9399516	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9399517	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9399519	0.88[ASN][1000 genomes]
rs9399520	0.88[ASN][1000 genomes]
rs9403622	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9403624	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9403625	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9403626	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9403628	0.86[ASN][1000 genomes]
rs9403629	0.90[ASN][1000 genomes]
rs9403630	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9403631	0.90[ASN][1000 genomes]
rs9403633	0.90[ASN][1000 genomes]
rs9403634	0.90[ASN][1000 genomes]
rs9497118	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9497128	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9688347	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9688355	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9688729	0.91[AMR][1000 genomes];0.87[EUR][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	nsv1016747	chr6:144917411-145599874	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv1850377	chr6:145199259-145319640	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	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	chr6:145222200-145224000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:145223400-145227000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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