Variant report

Variant	rs2207727
Chromosome Location	chr1:186492522-186492523
allele	A/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:42)

rs_ID	r²[population]
rs10798051	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10911877	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10911878	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10911888	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10911890	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10911892	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10911895	0.81[EUR][1000 genomes]
rs11580808	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11582183	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11805124	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12087470	0.82[EUR][1000 genomes]
rs12093901	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12402521	0.86[EUR][1000 genomes]
rs12728706	0.89[EUR][1000 genomes]
rs12750371	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1799957	0.89[EUR][1000 genomes]
rs1929092	0.87[EUR][1000 genomes]
rs2024761	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2180167	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2383508	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34396375	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35643079	0.89[EUR][1000 genomes]
rs36105782	0.89[EUR][1000 genomes]
rs3844242	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3901950	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4140433	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4567244	0.87[EUR][1000 genomes]
rs59547074	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6425035	0.83[AMR][1000 genomes]
rs6659683	0.86[EUR][1000 genomes]
rs6666413	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6666813	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6672836	0.87[EUR][1000 genomes]
rs6675505	0.87[EUR][1000 genomes]
rs6677346	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6680252	0.90[EUR][1000 genomes]
rs6689065	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6689727	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6694957	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7518525	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7536199	0.86[EUR][1000 genomes]
rs7556360	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004481	chr1:186095854-186750968	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv535223	chr1:186095854-186750968	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv1012164	chr1:186323867-186565995	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	esv2762201	chr1:186323879-186566007	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv832059	chr1:186464932-186639125	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr1:186470200-186493200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:186479000-186492600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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