Variant report

Variant	rs284753
Chromosome Location	chr5:35472600-35472601
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10041120	0.82[CEU][hapmap];0.85[EUR][1000 genomes]
rs10044118	0.85[EUR][1000 genomes]
rs10044161	0.85[EUR][1000 genomes]
rs11750298	0.81[ASN][1000 genomes]
rs1508659	0.89[EUR][1000 genomes]
rs1559274	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1559275	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16902130	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17618846	0.91[EUR][1000 genomes]
rs2036676	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2397843	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs26198	0.85[EUR][1000 genomes]
rs26199	0.85[EUR][1000 genomes]
rs26201	0.85[EUR][1000 genomes]
rs26204	0.85[EUR][1000 genomes]
rs27762	0.85[EUR][1000 genomes]
rs27940	0.83[EUR][1000 genomes]
rs28020	0.85[EUR][1000 genomes]
rs284692	0.85[EUR][1000 genomes]
rs284695	0.85[EUR][1000 genomes]
rs284742	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs284743	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs284744	0.81[ASN][1000 genomes]
rs284746	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs284747	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs284748	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs284749	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs284750	0.95[ASN][1000 genomes]
rs284751	0.82[ASN][1000 genomes]
rs284752	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs284754	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs284755	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs284756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs284758	0.81[ASN][1000 genomes]
rs284760	0.80[ASN][1000 genomes]
rs284762	0.81[ASN][1000 genomes]
rs284764	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs284765	0.95[CHB][hapmap];0.81[ASN][1000 genomes]
rs284766	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs284767	0.82[CEU][hapmap];0.82[JPT][hapmap]
rs284770	0.82[CEU][hapmap];0.82[JPT][hapmap]
rs32733	0.85[EUR][1000 genomes]
rs32754	0.82[EUR][1000 genomes]
rs32758	0.85[EUR][1000 genomes]
rs32789	0.85[EUR][1000 genomes]
rs4461609	0.81[ASN][1000 genomes]
rs457255	0.85[EUR][1000 genomes]
rs4703401	0.85[EUR][1000 genomes]
rs58530298	0.85[EUR][1000 genomes]
rs6451200	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6865370	0.85[EUR][1000 genomes]
rs6872931	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7705697	1.00[CEU][hapmap];0.90[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]

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	nsv1018541	chr5:35446209-35491185	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1030395	chr5:35446516-35491185	Enhancers Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35469200-35479400	Weak transcription	Pancreas	Pancrea
2	chr5:35471000-35475000	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr5:35471200-35473200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr5:35471200-35475800	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr5:35471600-35476400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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