Variant report

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11717433	0.83[ASN][1000 genomes]
rs11915356	0.91[AFR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12488103	0.89[ASN][1000 genomes]
rs12492983	0.89[ASN][1000 genomes]
rs12494582	0.84[ASN][1000 genomes]
rs12495362	0.84[ASN][1000 genomes]
rs1372071	0.86[ASN][1000 genomes]
rs17042920	0.86[ASN][1000 genomes]
rs2014490	0.88[ASN][1000 genomes]
rs34322012	0.82[ASN][1000 genomes]
rs4416363	0.82[ASN][1000 genomes]
rs4684305	0.88[ASN][1000 genomes]
rs4684306	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4685405	0.93[ASN][1000 genomes]
rs4685411	0.83[ASN][1000 genomes]
rs4685416	0.87[EUR][1000 genomes]
rs4685419	0.80[ASN][1000 genomes]
rs58679681	0.81[ASN][1000 genomes]
rs58750701	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58765457	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62246033	0.83[ASN][1000 genomes]
rs6806862	0.82[ASN][1000 genomes]
rs7617779	0.80[ASN][1000 genomes]
rs7639882	0.87[ASN][1000 genomes]
rs964576	0.88[ASN][1000 genomes]
rs9824172	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9825009	0.85[ASN][1000 genomes]
rs9879150	0.84[ASN][1000 genomes]
rs9883633	0.83[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv980048	chr3:16995372-17016178	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:16987400-17015600	Weak transcription	Aorta	Aorta
2	chr3:17005400-17015000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr3:17009200-17026600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr3:17009800-17015000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr3:17010400-17015600	Weak transcription	Right Ventricle	heart
6	chr3:17011000-17015000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr3:17013400-17016200	Weak transcription	Adipose Nuclei	Adipose

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