Variant report

Variant	rs7300750
Chromosome Location	chr12:22275061-22275062
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10492281	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10770890	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10770891	0.83[ASN][1000 genomes]
rs11046301	0.83[ASN][1000 genomes]
rs11502435	0.96[EUR][1000 genomes]
rs12303121	0.88[ASN][1000 genomes]
rs12306254	0.89[ASN][1000 genomes]
rs12829732	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12831501	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1861710	0.82[ASN][1000 genomes]
rs2080551	0.80[ASN][1000 genomes]
rs2080554	0.83[ASN][1000 genomes]
rs2193382	0.90[ASN][1000 genomes]
rs2193384	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2193385	0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2193386	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2193387	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2900495	0.84[ASN][1000 genomes]
rs2909067	0.84[ASN][1000 genomes]
rs2955495	0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2970797	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34299716	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34533494	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35253752	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35683388	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36064966	0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3937473	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6487285	0.83[ASN][1000 genomes]
rs7138641	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs71448629	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7296982	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7304110	0.84[ASN][1000 genomes]
rs7304537	0.81[ASN][1000 genomes]
rs7968893	0.95[ASN][1000 genomes]
rs7969364	0.83[ASN][1000 genomes]
rs9783526	0.94[EUR][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	esv2758298	chr12:22140834-22339299	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2759883	chr12:22140834-22736907	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:22274800-22275600	Enhancers	Fetal Stomach	stomach
2	chr12:22274800-22275800	Enhancers	Stomach Smooth Muscle	stomach
3	chr12:22274800-22276000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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