Variant report

Variant	rs4572561
Chromosome Location	chr2:183316895-183316896
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10178586	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10207132	0.85[GIH][hapmap]
rs10497601	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.94[TSI][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10497602	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs10497603	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs1125184	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.97[TSI][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12465662	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.94[TSI][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12465755	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12466618	0.88[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs12466937	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12468232	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];0.86[ASN][1000 genomes]
rs12468346	0.87[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs12470124	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12473820	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12474820	0.86[ASN][1000 genomes]
rs12475048	0.86[ASN][1000 genomes]
rs12478132	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.86[ASN][1000 genomes]
rs12479259	0.84[CEU][hapmap];1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs13417404	0.87[CHD][hapmap];0.81[TSI][hapmap]
rs1346775	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];0.86[ASN][1000 genomes]
rs1367203	0.85[GIH][hapmap]
rs1367204	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1430160	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1583112	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs16823249	0.82[YRI][hapmap]
rs16823275	0.85[ASN][1000 genomes]
rs17265166	0.86[ASN][1000 genomes]
rs17265189	0.88[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.86[ASN][1000 genomes]
rs17356207	0.85[GIH][hapmap]
rs17356296	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];0.86[ASN][1000 genomes]
rs17356303	0.87[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.86[ASN][1000 genomes]
rs17356331	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]
rs34103461	1.00[CHB][hapmap];0.96[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.93[ASN][1000 genomes]
rs34744930	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35809203	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35929267	0.83[EUR][1000 genomes]
rs4496292	0.88[CEU][hapmap];0.90[CHB][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs4666582	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4666584	0.83[EUR][1000 genomes]
rs4666585	1.00[CEU][hapmap];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4666834	0.85[EUR][1000 genomes]
rs4666835	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4666836	0.87[CHD][hapmap]
rs4666837	0.88[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs4666840	0.87[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs4666841	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs62187662	0.86[ASN][1000 genomes]
rs62187664	0.85[ASN][1000 genomes]
rs62187665	0.85[ASN][1000 genomes]
rs62187666	0.83[ASN][1000 genomes]
rs62188289	0.94[ASN][1000 genomes]
rs62188290	0.96[ASN][1000 genomes]
rs62188294	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62188295	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62188296	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62188297	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62189024	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62189025	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62189027	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62190676	0.86[ASN][1000 genomes]
rs62190677	0.85[ASN][1000 genomes]
rs62190678	0.86[ASN][1000 genomes]
rs62190679	0.86[ASN][1000 genomes]
rs62190680	0.86[ASN][1000 genomes]
rs62190681	0.86[ASN][1000 genomes]
rs62190682	0.86[ASN][1000 genomes]
rs62190684	0.85[ASN][1000 genomes]
rs6760364	1.00[CHB][hapmap];0.82[JPT][hapmap];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	nsv834481	chr2:183189758-183339577	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	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
4	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
5	esv3323574	chr2:183315057-183317155	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv2479479	chr2:183315368-183316896	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4572561	SSFA2	cis	cerebellum	SCAN
rs4572561	GABRA1	trans	parietal	SCAN
rs4572561	PPP1R1C	cis	parietal	SCAN

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183298800-183320800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:183313000-183321400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:183313000-183342600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:183313800-183320800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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