Variant report

Variant	rs751921
Chromosome Location	chr12:44795006-44795007
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 94 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10506245	1.00[JPT][hapmap]
rs10880632	1.00[ASN][1000 genomes]
rs11182486	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182490	1.00[ASN][1000 genomes]
rs11182493	1.00[ASN][1000 genomes]
rs11182495	1.00[ASN][1000 genomes]
rs11182496	1.00[ASN][1000 genomes]
rs11182497	0.94[ASN][1000 genomes]
rs11182501	0.94[ASN][1000 genomes]
rs11182517	0.87[ASN][1000 genomes]
rs11611818	0.94[ASN][1000 genomes]
rs11612521	1.00[ASN][1000 genomes]
rs12297907	1.00[ASN][1000 genomes]
rs12301564	1.00[ASN][1000 genomes]
rs12308701	0.94[ASN][1000 genomes]
rs12308760	1.00[ASN][1000 genomes]
rs12308816	0.88[ASN][1000 genomes]
rs12310262	0.94[ASN][1000 genomes]
rs12311228	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12317228	1.00[ASN][1000 genomes]
rs12318553	1.00[ASN][1000 genomes]
rs12319211	1.00[ASN][1000 genomes]
rs12319354	1.00[ASN][1000 genomes]
rs1353143	0.94[ASN][1000 genomes]
rs1353145	1.00[ASN][1000 genomes]
rs1353146	1.00[ASN][1000 genomes]
rs1353147	1.00[ASN][1000 genomes]
rs1493755	0.94[ASN][1000 genomes]
rs1527315	1.00[JPT][hapmap]
rs17094610	1.00[EUR][1000 genomes]
rs17094613	1.00[EUR][1000 genomes]
rs17094631	1.00[EUR][1000 genomes]
rs17094634	1.00[ASN][1000 genomes]
rs17094647	0.96[EUR][1000 genomes]
rs17094695	0.87[ASN][1000 genomes]
rs17094740	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs17121322	1.00[ASN][1000 genomes]
rs17121326	0.96[EUR][1000 genomes]
rs1716605	1.00[JPT][hapmap]
rs1716609	1.00[JPT][hapmap]
rs1726884	1.00[JPT][hapmap]
rs1726889	1.00[JPT][hapmap]
rs1798023	1.00[JPT][hapmap]
rs1798032	1.00[JPT][hapmap]
rs1873978	1.00[ASN][1000 genomes]
rs1873980	1.00[ASN][1000 genomes]
rs1873981	0.94[ASN][1000 genomes]
rs4639992	1.00[JPT][hapmap]
rs4768559	1.00[JPT][hapmap]
rs55781129	0.87[ASN][1000 genomes]
rs55962853	0.87[ASN][1000 genomes]
rs56020032	0.87[ASN][1000 genomes]
rs56115011	1.00[ASN][1000 genomes]
rs56204564	1.00[EUR][1000 genomes]
rs56318423	0.87[ASN][1000 genomes]
rs57115451	0.89[EUR][1000 genomes]
rs59255697	0.87[ASN][1000 genomes]
rs60837979	0.87[ASN][1000 genomes]
rs68107418	0.94[ASN][1000 genomes]
rs7132743	0.94[ASN][1000 genomes]
rs7134756	1.00[ASN][1000 genomes]
rs7299010	0.87[ASN][1000 genomes]
rs7302676	0.87[ASN][1000 genomes]
rs73094334	1.00[ASN][1000 genomes]
rs7309948	0.81[ASN][1000 genomes]
rs7314412	1.00[JPT][hapmap]
rs74085067	0.87[ASN][1000 genomes]
rs74085071	0.87[ASN][1000 genomes]
rs74085073	0.87[ASN][1000 genomes]
rs74085078	0.87[ASN][1000 genomes]
rs7953681	0.85[CEU][hapmap];1.00[MEX][hapmap];0.87[ASN][1000 genomes]
rs7957832	0.87[ASN][1000 genomes]
rs7958300	0.85[CEU][hapmap];0.87[ASN][1000 genomes]
rs7958770	0.85[CEU][hapmap];0.87[ASN][1000 genomes]
rs7960681	0.87[ASN][1000 genomes]
rs7962332	1.00[ASN][1000 genomes]
rs7964751	1.00[ASN][1000 genomes]
rs7965110	1.00[ASN][1000 genomes]
rs7965383	1.00[ASN][1000 genomes]
rs7969400	1.00[ASN][1000 genomes]
rs7969428	1.00[ASN][1000 genomes]
rs7969466	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs7969614	0.94[ASN][1000 genomes]
rs7970601	0.87[ASN][1000 genomes]
rs7971520	0.87[ASN][1000 genomes]
rs7972882	1.00[ASN][1000 genomes]
rs7978776	1.00[ASN][1000 genomes]
rs7979642	0.85[CEU][hapmap];0.87[ASN][1000 genomes]
rs840773	1.00[JPT][hapmap]
rs840774	1.00[JPT][hapmap]
rs859016	1.00[JPT][hapmap]
rs863482	1.00[JPT][hapmap]

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	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1038498	chr12:44679455-44816572	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 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	chr12:44792600-44796600	Weak transcription	Fetal Intestine Large	intestine

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