Variant report

Variant	rs1867633
Chromosome Location	chr8:69317537-69317538
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs12541312	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12545937	0.90[ASN][1000 genomes]
rs12547748	0.94[EUR][1000 genomes]
rs1517129	0.88[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1517130	0.88[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs16919092	0.88[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs16934487	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs16934510	0.88[CHB][hapmap];1.00[JPT][hapmap]
rs16934519	1.00[GIH][hapmap]
rs16934533	0.89[MEX][hapmap]
rs16934546	0.89[MEX][hapmap]
rs16934573	0.87[TSI][hapmap];0.94[EUR][1000 genomes]
rs1980177	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2255882	0.88[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2591019	0.88[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2591020	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2591022	0.85[ASN][1000 genomes]
rs2676633	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2676634	0.85[ASN][1000 genomes]
rs2676648	0.88[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2676649	0.90[ASN][1000 genomes]
rs2676650	0.88[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2676652	0.88[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2676654	0.88[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2676656	0.90[ASN][1000 genomes]
rs2944715	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs34225325	0.88[EUR][1000 genomes]
rs3812450	1.00[GIH][hapmap];1.00[JPT][hapmap]
rs4737257	0.88[EUR][1000 genomes]
rs56708665	0.85[ASN][1000 genomes]
rs58125593	0.98[ASN][1000 genomes]
rs59098392	1.00[ASN][1000 genomes]
rs59134336	1.00[ASN][1000 genomes]
rs61482308	0.94[EUR][1000 genomes]
rs6995683	0.89[MEX][hapmap]
rs6999119	1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7000104	1.00[CEU][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7005081	1.00[GIH][hapmap]
rs73260728	0.94[EUR][1000 genomes]
rs73260731	0.94[EUR][1000 genomes]
rs73260764	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7843010	0.89[MEX][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv508512	chr8:69268794-69324532	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1023810	chr8:69308665-69440129	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv539644	chr8:69308665-69440129	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69317200-69342600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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