Variant report

Variant	rs1226735
Chromosome Location	chr1:45646318-45646319
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs1144868	0.82[ASN][1000 genomes]
rs11806438	0.83[ASN][1000 genomes]
rs11810239	0.82[ASN][1000 genomes]
rs1226670	0.83[ASN][1000 genomes]
rs1226733	0.85[ASN][1000 genomes]
rs1226734	0.85[ASN][1000 genomes]
rs1226746	0.83[ASN][1000 genomes]
rs1226747	0.83[ASN][1000 genomes]
rs1226748	0.83[ASN][1000 genomes]
rs1226914	0.80[ASN][1000 genomes]
rs1782459	0.81[ASN][1000 genomes]
rs1938300	0.82[ASN][1000 genomes]
rs1938301	0.82[ASN][1000 genomes]
rs1938303	0.83[ASN][1000 genomes]
rs1938304	0.82[ASN][1000 genomes]
rs2088956	0.82[ASN][1000 genomes]
rs2105458	0.83[ASN][1000 genomes]
rs2356302	0.82[ASN][1000 genomes]
rs238249	0.83[ASN][1000 genomes]
rs2997461	0.83[ASN][1000 genomes]
rs2997465	0.82[ASN][1000 genomes]
rs3009968	0.82[ASN][1000 genomes]
rs3009969	0.82[ASN][1000 genomes]
rs3009974	0.83[ASN][1000 genomes]
rs3009979	0.83[ASN][1000 genomes]
rs34134455	0.83[ASN][1000 genomes]
rs346684	0.83[ASN][1000 genomes]
rs346687	0.82[ASN][1000 genomes]
rs346693	0.83[ASN][1000 genomes]
rs346695	0.83[ASN][1000 genomes]
rs346696	0.82[ASN][1000 genomes]
rs346697	0.83[ASN][1000 genomes]
rs346698	0.83[ASN][1000 genomes]
rs346700	0.83[ASN][1000 genomes]
rs346701	0.83[ASN][1000 genomes]
rs346702	0.83[ASN][1000 genomes]
rs346705	0.83[ASN][1000 genomes]
rs346706	0.83[ASN][1000 genomes]
rs346707	0.83[ASN][1000 genomes]
rs346712	0.83[ASN][1000 genomes]
rs346716	0.83[ASN][1000 genomes]
rs346717	0.83[ASN][1000 genomes]
rs346719	0.83[ASN][1000 genomes]
rs346721	0.83[ASN][1000 genomes]
rs346723	0.82[ASN][1000 genomes]
rs346724	0.83[ASN][1000 genomes]
rs346729	0.83[ASN][1000 genomes]
rs346732	0.83[ASN][1000 genomes]
rs346733	0.83[ASN][1000 genomes]
rs346734	0.83[ASN][1000 genomes]
rs346735	0.83[ASN][1000 genomes]
rs346736	0.83[ASN][1000 genomes]
rs346737	0.82[ASN][1000 genomes]
rs3738246	0.82[ASN][1000 genomes]
rs3850855	0.82[ASN][1000 genomes]
rs3850856	0.83[ASN][1000 genomes]
rs415536	0.83[ASN][1000 genomes]
rs454624	0.83[ASN][1000 genomes]
rs4660295	0.83[ASN][1000 genomes]
rs4660834	0.82[ASN][1000 genomes]
rs4660839	0.83[ASN][1000 genomes]
rs4660841	0.83[ASN][1000 genomes]
rs56363452	0.83[ASN][1000 genomes]
rs56791336	0.83[ASN][1000 genomes]
rs58374842	0.83[ASN][1000 genomes]
rs58934647	0.83[ASN][1000 genomes]
rs61789780	0.83[ASN][1000 genomes]
rs61789781	0.83[ASN][1000 genomes]
rs6429557	0.82[ASN][1000 genomes]
rs6688318	0.82[ASN][1000 genomes]
rs6702327	0.82[ASN][1000 genomes]
rs72684493	0.83[ASN][1000 genomes]
rs974143	0.83[ASN][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	nsv529677	chr1:45179509-45748571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	424 gene(s)	inside rSNPs	diseases
2	nsv1002026	chr1:45187594-45758048	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	386 gene(s)	inside rSNPs	diseases
3	nsv915644	chr1:45282802-45696079	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
4	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
5	nsv945918	chr1:45642615-45660743	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45645600-45662600	Weak transcription	HepG2	liver

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