Variant report

Variant	rs7827412
Chromosome Location	chr8:125077425-125077426
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10094266	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10094533	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10102566	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10106600	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10113693	0.85[EUR][1000 genomes]
rs10113772	0.86[EUR][1000 genomes]
rs1073178	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1075051	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10808530	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10808531	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10956163	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10956164	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12541155	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12545670	0.84[EUR][1000 genomes]
rs13251412	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13254252	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13254498	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13258808	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13258930	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13261097	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13263969	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13269044	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2069078	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4294164	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4330676	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4345538	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4374969	0.81[ASN][1000 genomes]
rs4404895	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4410885	0.88[EUR][1000 genomes]
rs4412351	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4430074	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4446721	0.81[ASN][1000 genomes]
rs4460351	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4483139	0.94[ASN][1000 genomes]
rs4483140	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4484683	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4500064	0.83[ASN][1000 genomes]
rs4510842	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4623400	0.81[ASN][1000 genomes]
rs4871460	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4871461	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4871462	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs59583746	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6470216	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6470217	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6470218	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6470219	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6470220	0.88[EUR][1000 genomes]
rs6470221	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6987082	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6991629	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7005123	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7007739	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7009406	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7010375	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7012186	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7013226	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7815620	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7815768	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7816075	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7822018	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7822412	0.90[AMR][1000 genomes]
rs7822557	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7825506	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7826405	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7832499	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7836974	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9297683	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9297684	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9297685	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9643188	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]

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	nsv6375	chr8:125056543-125087258	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv612144	chr8:125057728-125206503	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1023183	chr8:125060532-125206445	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv948556	chr8:125067187-125204721	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125052600-125083600	Weak transcription	Gastric	stomach
2	chr8:125064400-125078600	Weak transcription	Stomach Mucosa	stomach
3	chr8:125074800-125095400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:125076800-125121800	Weak transcription	Fetal Stomach	stomach

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