Variant report

Variant	rs17356331
Chromosome Location	chr2:183352830-183352831
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10171703	0.85[JPT][hapmap]
rs10178586	0.86[CEU][hapmap];0.80[CHB][hapmap];0.83[JPT][hapmap]
rs10497601	0.86[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap]
rs10497602	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs10497603	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1125184	0.86[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];0.87[MEX][hapmap];0.85[ASN][1000 genomes]
rs12465662	0.86[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap]
rs12466618	1.00[CEU][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12468232	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12468346	1.00[CEU][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12474820	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12475048	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12478132	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12479259	1.00[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13417404	0.87[CHD][hapmap];0.85[JPT][hapmap]
rs1346775	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1367204	0.86[CEU][hapmap];0.80[CHB][hapmap];0.83[JPT][hapmap]
rs1430141	0.85[JPT][hapmap]
rs1430160	0.86[CEU][hapmap];0.80[CHB][hapmap];0.83[JPT][hapmap]
rs1583112	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1594304	0.85[JPT][hapmap]
rs16823275	0.85[ASN][1000 genomes]
rs16823285	0.85[JPT][hapmap]
rs17265166	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17265189	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17356296	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17356303	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34103461	0.80[CHB][hapmap];0.97[CHD][hapmap];0.83[JPT][hapmap]
rs4496292	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs4572561	0.86[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];0.81[MEX][hapmap];0.83[ASN][1000 genomes]
rs4666582	0.86[CEU][hapmap];0.80[CHB][hapmap];0.83[JPT][hapmap]
rs4666585	0.83[CEU][hapmap]
rs4666835	0.86[CEU][hapmap];0.80[CHB][hapmap];0.83[JPT][hapmap]
rs4666836	0.87[CHD][hapmap];0.85[JPT][hapmap]
rs4666837	1.00[CEU][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4666838	0.84[JPT][hapmap]
rs4666840	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4666841	1.00[CEU][hapmap];0.80[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.86[MKK][hapmap];0.89[TSI][hapmap];0.85[AFR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62187662	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62187664	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62187665	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62187666	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62188294	0.82[ASN][1000 genomes]
rs62188295	0.85[ASN][1000 genomes]
rs62188296	0.85[ASN][1000 genomes]
rs62188297	0.85[ASN][1000 genomes]
rs62189024	0.85[ASN][1000 genomes]
rs62190676	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62190677	0.85[ASN][1000 genomes]
rs62190678	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62190679	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62190680	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62190681	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62190682	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62190684	0.85[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	nsv533782	chr2:183059730-183500040	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	esv2830429	chr2:183300759-183545378	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183343200-183353800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:183347800-183355800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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