Variant report

Variant	rs73184562
Chromosome Location	chr12:86245024-86245025
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 132 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:126)

rs_ID	r²[population]
rs10506918	0.89[ASN][1000 genomes]
rs10779216	0.89[ASN][1000 genomes]
rs10863083	0.89[ASN][1000 genomes]
rs10863085	1.00[ASN][1000 genomes]
rs10863086	0.89[ASN][1000 genomes]
rs11117042	0.89[ASN][1000 genomes]
rs11117050	0.89[ASN][1000 genomes]
rs11117051	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11117052	0.89[ASN][1000 genomes]
rs11117053	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11117057	0.89[ASN][1000 genomes]
rs11117064	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11117065	0.81[ASN][1000 genomes]
rs11503595	0.89[ASN][1000 genomes]
rs11611664	0.89[ASN][1000 genomes]
rs11613243	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11614033	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11614830	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11614924	0.89[ASN][1000 genomes]
rs11615953	0.80[EUR][1000 genomes]
rs11832503	0.89[ASN][1000 genomes]
rs11832948	0.81[ASN][1000 genomes]
rs11832992	0.89[ASN][1000 genomes]
rs11833148	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11837152	0.89[ASN][1000 genomes]
rs11838160	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12297441	0.89[ASN][1000 genomes]
rs12300728	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12305828	0.89[ASN][1000 genomes]
rs12307686	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12308839	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12308898	0.89[ASN][1000 genomes]
rs12309296	0.89[ASN][1000 genomes]
rs12309878	0.89[ASN][1000 genomes]
rs12313775	0.89[ASN][1000 genomes]
rs12314274	0.89[ASN][1000 genomes]
rs12314318	0.89[ASN][1000 genomes]
rs1349060	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1349061	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1349063	0.81[ASN][1000 genomes]
rs1448096	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1448097	0.89[ASN][1000 genomes]
rs1448098	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1448099	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1584368	0.89[ASN][1000 genomes]
rs1584369	0.89[ASN][1000 genomes]
rs17280216	0.86[ASN][1000 genomes]
rs17280483	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17280643	0.89[ASN][1000 genomes]
rs17280790	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs17345787	0.86[ASN][1000 genomes]
rs17345849	0.86[ASN][1000 genomes]
rs17345975	0.89[ASN][1000 genomes]
rs17346231	0.89[ASN][1000 genomes]
rs1900700	0.89[ASN][1000 genomes]
rs1900701	0.89[ASN][1000 genomes]
rs2197769	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2234762	0.81[ASN][1000 genomes]
rs4274268	0.89[ASN][1000 genomes]
rs4362214	0.89[ASN][1000 genomes]
rs4436622	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4488288	0.89[ASN][1000 genomes]
rs4540904	0.86[ASN][1000 genomes]
rs4919770	0.89[ASN][1000 genomes]
rs4919771	0.89[ASN][1000 genomes]
rs4919779	0.89[ASN][1000 genomes]
rs56082822	0.89[ASN][1000 genomes]
rs57278040	0.89[ASN][1000 genomes]
rs57614821	0.86[ASN][1000 genomes]
rs59445394	0.89[ASN][1000 genomes]
rs60986162	0.89[ASN][1000 genomes]
rs61928909	0.85[ASN][1000 genomes]
rs61928919	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs61928920	0.96[ASN][1000 genomes]
rs61928955	0.86[ASN][1000 genomes]
rs61930064	0.89[ASN][1000 genomes]
rs61930066	0.89[ASN][1000 genomes]
rs61930067	0.89[ASN][1000 genomes]
rs61930068	0.89[ASN][1000 genomes]
rs61930074	0.89[ASN][1000 genomes]
rs61930076	0.89[ASN][1000 genomes]
rs61930078	0.89[ASN][1000 genomes]
rs61930132	0.89[ASN][1000 genomes]
rs61930137	0.89[ASN][1000 genomes]
rs61930139	0.89[ASN][1000 genomes]
rs61930140	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61930862	0.89[ASN][1000 genomes]
rs61930864	0.89[ASN][1000 genomes]
rs61930865	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61930873	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6539923	0.89[ASN][1000 genomes]
rs6539924	0.89[ASN][1000 genomes]
rs6539925	0.89[ASN][1000 genomes]
rs6539926	0.89[ASN][1000 genomes]
rs6539927	0.89[ASN][1000 genomes]
rs6539928	0.86[ASN][1000 genomes]
rs6539929	0.89[ASN][1000 genomes]
rs6539931	0.89[ASN][1000 genomes]
rs6539932	0.89[ASN][1000 genomes]
rs6539933	0.89[ASN][1000 genomes]
rs7133591	0.89[ASN][1000 genomes]
rs7134732	0.89[ASN][1000 genomes]
rs7137596	0.89[ASN][1000 genomes]
rs7297996	0.86[ASN][1000 genomes]
rs7298536	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7299285	0.89[ASN][1000 genomes]
rs7302741	0.89[ASN][1000 genomes]
rs7303330	0.89[ASN][1000 genomes]
rs7304873	0.89[ASN][1000 genomes]
rs7308229	0.89[ASN][1000 genomes]
rs7309500	0.89[ASN][1000 genomes]
rs7311532	0.89[ASN][1000 genomes]
rs7316772	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs73176583	0.89[ASN][1000 genomes]
rs7953318	0.89[ASN][1000 genomes]
rs7953353	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs7957170	0.89[ASN][1000 genomes]
rs7960130	0.89[ASN][1000 genomes]
rs7965388	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7967183	0.89[ASN][1000 genomes]
rs7968248	0.89[ASN][1000 genomes]
rs7970081	0.89[ASN][1000 genomes]
rs7970732	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7970842	0.89[ASN][1000 genomes]
rs7974167	0.88[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9788152	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052187	chr12:85954455-86278200	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv541560	chr12:85954455-86278200	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1049443	chr12:86185887-86272493	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	n/a
5	esv1797806	chr12:86198935-86425608	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv1036914	chr12:86201703-86272493	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86243200-86249200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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