Variant report

Variant	rs10029040
Chromosome Location	chr4:21718069-21718070
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 105 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs10002096	0.82[ASN][1000 genomes]
rs10021133	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10516398	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10516400	0.90[ASN][1000 genomes]
rs10805230	0.86[ASN][1000 genomes]
rs10938854	0.93[ASN][1000 genomes]
rs10938860	0.85[ASN][1000 genomes]
rs11723231	0.90[ASN][1000 genomes]
rs11725634	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11725680	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11728958	0.90[ASN][1000 genomes]
rs11730531	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11731098	0.86[ASN][1000 genomes]
rs11734604	0.93[ASN][1000 genomes]
rs11736882	0.93[ASN][1000 genomes]
rs11737531	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11931923	0.86[ASN][1000 genomes]
rs11938269	0.93[ASN][1000 genomes]
rs11944162	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12503772	0.90[ASN][1000 genomes]
rs13104527	0.82[ASN][1000 genomes]
rs13105122	0.85[ASN][1000 genomes]
rs13105154	0.93[ASN][1000 genomes]
rs13112610	0.85[ASN][1000 genomes]
rs13115987	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13119994	0.90[ASN][1000 genomes]
rs13128189	0.90[ASN][1000 genomes]
rs13129819	0.85[ASN][1000 genomes]
rs13132296	0.93[ASN][1000 genomes]
rs13135188	0.93[ASN][1000 genomes]
rs13135698	0.93[ASN][1000 genomes]
rs13141904	0.93[ASN][1000 genomes]
rs13142511	0.80[ASN][1000 genomes]
rs13143578	0.93[ASN][1000 genomes]
rs13146273	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13147352	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1380271	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1380272	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1398835	0.85[ASN][1000 genomes]
rs1459279	0.90[ASN][1000 genomes]
rs1459280	0.90[ASN][1000 genomes]
rs168626	0.86[ASN][1000 genomes]
rs17496681	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17496959	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17497844	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17497900	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17498614	0.93[ASN][1000 genomes]
rs17563311	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17563769	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17563824	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17564865	0.93[ASN][1000 genomes]
rs17566434	0.90[ASN][1000 genomes]
rs1824368	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1841187	0.90[ASN][1000 genomes]
rs1841188	0.90[ASN][1000 genomes]
rs184860	0.81[ASN][1000 genomes]
rs2044809	0.90[ASN][1000 genomes]
rs2137650	0.86[ASN][1000 genomes]
rs2175779	0.85[ASN][1000 genomes]
rs2175780	0.85[ASN][1000 genomes]
rs2323128	0.86[ASN][1000 genomes]
rs34099045	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34375823	0.93[ASN][1000 genomes]
rs34708714	0.90[ASN][1000 genomes]
rs34839938	0.86[ASN][1000 genomes]
rs34945659	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35146316	0.85[ASN][1000 genomes]
rs35161937	0.93[ASN][1000 genomes]
rs35175333	0.90[ASN][1000 genomes]
rs35215732	0.85[ASN][1000 genomes]
rs35489277	0.91[ASN][1000 genomes]
rs35719625	0.88[ASN][1000 genomes]
rs35733545	0.93[ASN][1000 genomes]
rs35827665	0.86[ASN][1000 genomes]
rs35842590	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35921228	0.83[ASN][1000 genomes]
rs35937671	0.90[ASN][1000 genomes]
rs360698	0.86[ASN][1000 genomes]
rs4455402	0.86[ASN][1000 genomes]
rs4618303	0.90[ASN][1000 genomes]
rs4631029	0.90[ASN][1000 genomes]
rs57134420	0.80[ASN][1000 genomes]
rs57505034	0.90[ASN][1000 genomes]
rs60628330	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6448076	0.93[ASN][1000 genomes]
rs6448091	0.90[ASN][1000 genomes]
rs6819627	0.80[ASN][1000 genomes]
rs6834778	0.93[ASN][1000 genomes]
rs6839725	0.80[ASN][1000 genomes]
rs6839776	0.80[ASN][1000 genomes]
rs71607091	0.93[ASN][1000 genomes]
rs71607093	0.90[ASN][1000 genomes]
rs71607096	0.86[ASN][1000 genomes]
rs7656546	0.90[ASN][1000 genomes]
rs7659552	0.91[ASN][1000 genomes]
rs7661087	0.85[ASN][1000 genomes]
rs7662958	0.93[ASN][1000 genomes]
rs7684151	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7695756	0.93[ASN][1000 genomes]
rs9884203	0.82[ASN][1000 genomes]
rs9884843	0.82[ASN][1000 genomes]
rs9995230	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817467	chr4:21602921-22422816	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv878751	chr4:21712050-21793807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv3420109	chr4:21714454-21718652	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21712400-21718400	Weak transcription	Ovary	ovary

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